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HCPCS Code

HCPCS code K0554 – Continuous glucose monitor receiver


Code Definition

K0554 is the deleted HCPCS Level II code for receiver (monitor), dedicated, for use with therapeutic glucose continuous monitor system. CMS ended it on December 31, 2022, so it is not billable for any date of service from January 1, 2023.

Its replacement is E2103, the receiver code for a non-adjunctive CGM, with monthly supplies under A4239. An adjunctive CGM bills as E2102 for the receiver and A4238 for supplies, under Glucose Monitors LCD L33822.

Level
Level II
Category
K — DME temporary codes
Status
Deleted, effective 31 December 2022
Billable
No
Code also known as
CGM receiver, therapeutic CGM monitor, non-adjunctive CGM device
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Key takeaways

Key takeaways

K0554 was deleted effective December 31, 2022, so it is not billable for any date of service from January 1, 2023.

A non-adjunctive CGM receiver now bills as E2103, with its monthly supply allowance under A4239.

An adjunctive CGM bills as E2102 for the receiver and A4238 for supplies, with up to three monthly units per 90 days.

Coverage runs on one national LCD, L33822, and Medicare applies no prior authorization to these CGM codes.

HCPCS code K0554: a deleted CGM receiver code

HCPCS code K0554 described a receiver (monitor), dedicated, for use with a therapeutic glucose continuous monitor system. CMS deleted it effective December 31, 2022, and cross-walked it to E2103. The deletion appears in the CMS HCPCS quarterly update files.

A claim that carries K0554 for a date of service on or after January 1, 2023 is rejected as an invalid code. If you still see it in a charge master, a fee table, or a supplier template, replace it before the next billing cycle.

Field Detail
Code K0554
Official descriptor Receiver (monitor), dedicated, for use with therapeutic glucose continuous monitor system
Code type HCPCS Level II, K-series (temporary DME code)
Status Deleted, effective December 31, 2022
Last valid date of service December 31, 2022
Replacement receiver code E2103 (non-adjunctive, nonimplanted CGM or receiver)
Replacement supply code A4239 (non-adjunctive CGM supply allowance, one month per unit)

Why K0554 was deleted and what replaced it

K0553 and K0554 were the temporary codes for therapeutic CGMs. K0553 was the monthly supply allowance and K0554 was the receiver. Both covered the same type of device, so they never split adjunctive from non-adjunctive systems.

The adjunctive codes, E2102 and A4238, had existed since April 1, 2022. From January 1, 2023, E2103 and A4239 took over the non-adjunctive role, which completed the split. The revised Glucose Monitors LCD L33822 uses them for every CGM Medicare covers under the DME benefit.

  • K0554 (receiver): cross-walked to E2103, the non-adjunctive receiver code
  • K0553 (supply allowance): cross-walked to A4239, the non-adjunctive supply allowance
  • Adjunctive systems: already billed as E2102 for the receiver and A4238 for supplies, both effective April 1, 2022

Replacement codes: E2103, A4239, E2102, and A4238

A non-adjunctive CGM can be used to make treatment decisions without a confirming fingerstick. An adjunctive CGM needs a fingerstick reading before the patient changes treatment. The device’s FDA labeling decides which pair of codes you bill.

Code What it describes Billing unit
E2103 Non-adjunctive, nonimplanted CGM or receiver Per device
A4239 Supply allowance for a non-adjunctive, nonimplanted CGM, including all supplies and accessories One month = one unit
E2102 Adjunctive, nonimplanted CGM or receiver Per device
A4238 Supply allowance for an adjunctive, nonimplanted CGM, including all supplies and accessories One month = one unit

Bill the supply allowance in monthly units, up to three units per 90 days. A4239 already includes sensors, transmitters, a home blood glucose monitor (BGM), and its supplies, so none of them is billed separately. That no-unbundling rule applies to A4239 only.

A4238 users may bill the BGM and its test supplies separately, such as lancets under A4259. Implanted CGMs fall outside all four codes, since each descriptor is limited to nonimplanted systems.

Pro Tip

Search your billing system for K0553 and K0554 before your next DME claim run. A deleted code left in a supplier template or fee table will reject every claim it touches. The fix is a one-line mapping to E2103 or A4239.

Medicare coverage criteria under LCD L33822

Medicare covers a CGM and its supply allowance under the Part B DME benefit when the patient meets all five initial criteria in LCD L33822:

  1. The patient has diabetes mellitus
  2. The patient or caregiver has had sufficient training on using the prescribed CGM
  3. The CGM is prescribed in line with its FDA indications for use
  4. The patient is insulin-treated, or has a documented history of problematic hypoglycemia
  5. Within the six months before ordering, the treating practitioner had an in-person or Medicare-approved telehealth visit to confirm the criteria above

The training criterion refers to training on the CGM itself. It is not a diabetes self-management training (DSMT) requirement. For continued coverage, the practitioner sees the patient every six months to review CGM use and diabetes control, in person or by Medicare-approved telehealth.

Problematic hypoglycemia means recurrent level 2 events that persist despite treatment changes, or at least one level 3 event that needed help from another person. Code the diabetes diagnosis to full specificity and check it against the ICD-10-CM list in Policy Article A52464.

Who administers the LCD

L33822 is a single national LCD shared by all four DME Medicare Administrative Contractors (MACs). Noridian covers Jurisdictions A and D, and CGS covers Jurisdictions B and C. The coverage criteria are the same in every jurisdiction.

Documentation to keep on file

The supplier needs each of these on file before the claim goes out. Keeping HIPAA-compliant records for every item also protects you on a post-payment audit.

  • Standard written order (SWO): from the treating practitioner, naming the CGM receiver or supply allowance ordered
  • Visit note: the in-person or telehealth visit within six months before the order, showing the coverage criteria were met
  • Insulin or hypoglycemia evidence: the insulin regimen, or the documented hypoglycemic events
  • CGM training: a record that the patient or caregiver was trained on the prescribed device
  • Proof of delivery: signed by the patient or an authorized representative
  • Refill records: each supply allowance shipment, to support the three-units-per-90-days limit

No Medicare prior authorization applies to E2102, E2103, A4238, or A4239. Commercial and Medicare Advantage plans set their own rules, so check each payer before delivery.

Modifiers for CGM receivers and supply allowances

Every CGM claim line carries KX or KS, never both, depending on insulin status. CG depends on the coverage criteria, and KF depends on the code billed and the device’s FDA class.

Modifier Meaning When to use it
KX Requirements in the medical policy have been met The patient is insulin-treated (KX or KS is required on every claim line)
KS Glucose monitor supply for a patient not treated with insulin The patient qualifies through problematic hypoglycemia instead of insulin use
KF Item designated by the FDA as a Class III device Required on every E2102 and A4238 line, or the line is rejected. On E2103 and A4239, add it only when the CGM is an FDA Class III device.
CG Policy criteria applied Append to E2103, A4239, E2102, or A4238 only when all five LCD coverage criteria are met, initial and continued

Never put KX and KS on the same claim line. Confirm the current modifier set, including the CG rule, against Policy Article A52464 before you submit. The chart below puts the code pair and modifier choices for each device type side by side.

Decision chart for billing a CGM after K0554.
The FDA labeling sets the code pair, while insulin status and the five coverage criteria set the modifiers. Rules from CMS Policy Article A52464.

How to bill a CGM receiver today

Billing a CGM after the K0554 deletion follows the standard DMEPOS claim path. The steps below apply to both non-adjunctive and adjunctive systems.

  1. Confirm the device’s FDA labeling to choose E2103 and A4239, or E2102 and A4238
  2. Check that the visit note, SWO, and CGM training record are on file
  3. Deliver the receiver and get a signed proof of delivery
  4. Submit the claim on the 837P (or CMS-1500) to the DME MAC for the patient’s state
  5. Append KX or KS to every line, never both, plus CG when all five LCD criteria are met
  6. Add KF to every E2102 and A4238 line, and to E2103 or A4239 only for an FDA Class III device
  7. Bill the supply allowance in monthly units, up to three units per 90 days
  8. Retain the full documentation file for at least seven years
Pabau payment screen showing remittance totals and paid, unpaid and reissued claim statuses
Pabau, the practice software we build, shows each claim’s payment status against its remittance, so an unpaid CGM claim stands out for follow-up.

Common reasons CGM claims are denied

Most CGM denials trace back to a deleted code, a mismatched code pair, or a missing document. Each one below can be corrected before resubmission.

Denial reason Root cause Corrective action
Invalid HCPCS code K0554 or K0553 billed for a date of service after December 31, 2022 Replace with E2103 or A4239 (or E2102 or A4238) and resubmit
Code pair mismatch Adjunctive codes billed for a non-adjunctive device, or the reverse Check the FDA labeling and bill the matching receiver and supply codes
Wrong or missing modifier KX or KS absent, both on one line, or KF missing on an E2102, A4238, or Class III line Correct the modifier to match the insulin status and device class
Coverage criteria not documented No qualifying visit within six months, or no insulin or hypoglycemia evidence Add the missing visit note or evidence and appeal
Units over the limit More than three supply allowance units billed in 90 days Rebill within the limit and align refill dates
Unbundled supplies Sensors, transmitters, a BGM, or its test supplies billed alongside A4239 Remove the separate lines, since A4239 already includes them. A4238 users may bill BGM supplies separately.

The supplier bills the equipment codes, which sit with the other DME items in our HCPCS code library. The treating practitioner bills the clinical CGM services under CPT codes such as 95251, on a separate claim. The AAPC HCPCS code lookup is a quick way to confirm any descriptor below.

Code Description Status or use
K0553 Supply allowance for therapeutic CGM, one month per unit Deleted December 31, 2022; replaced by A4239
E2103 Non-adjunctive, nonimplanted CGM or receiver Active; replaces K0554
A4239 Non-adjunctive CGM supply allowance, one month per unit Active; replaces K0553
E2102 Adjunctive, nonimplanted CGM or receiver Active
A4238 Adjunctive CGM supply allowance, one month per unit Active
95250 Ambulatory CGM, sensor placement, hook-up, calibration, patient training, and printout Billed by the practitioner
95251 Ambulatory CGM, analysis, interpretation, and report Billed by the practitioner, once per month

Medicare reimbursement for CGM receivers

K0554 has no current Medicare rate, because a deleted code has no fee schedule amount. E2103 and its siblings are paid from the DMEPOS fee schedule, which sets allowables by state.

Pull current amounts from the CMS DMEPOS fee schedule files instead of the Physician Fee Schedule. CMS updates those files each quarter, with the main annual update taking effect on January 1. Commercial payers set their own CGM rates in your contract.

How Pabau supports CGM claim tracking

Most CGM denials start with a deleted code or a missing document that nobody spotted before submission. Pabau keeps the visit note, order, and claim in one patient record, so your team can check them side by side.

Your team still selects the codes and diagnoses. Pabau’s claims management software then submits the claim electronically and tracks its status, so a rejection shows up quickly for correction.

Track every CGM claim from submission to payment

Pabau submits your claims electronically and tracks each one, so your team can spot a rejected CGM claim and correct it quickly.

Pabau claims management dashboard

Conclusion

Treat K0554 as a retired code. Any CGM claim built on it for a 2023 or later service date will reject, and it cannot be fixed with a modifier.

Map each system to the right replacement pair, E2103 and A4239 or E2102 and A4238. Then document the five L33822 criteria before the first claim goes out.

Pabau keeps those records and the claim history in one place, next to each patient’s visit notes. Book a demo to see how Pabau helps your team submit and track CGM claims.

Continue your research

Continue your research

Billing the old supply allowance code? HCPCS code K0553 explains the deleted CGM supply allowance and how A4239 replaced it.

Billing a CGM that falls outside the DME benefit? HCPCS code A9278 covers external CGM receivers that do not meet the Medicare DME definition.

Billing fingerstick supplies for a patient on a CGM? HCPCS code A4259 explains when lancets are payable and when an allowance already covers them.

Billing the practitioner side of CGM? CPT code 95251 covers monthly analysis and interpretation of CGM data.

Billing diabetes education alongside the supplies? HCPCS code G0109 covers group self-management training and its frequency limits.

Frequently asked questions

Is HCPCS code K0554 still billable?

No. CMS deleted K0554 effective December 31, 2022, so it cannot be billed for any date of service from January 1, 2023. Claims that carry it are rejected as an invalid code.

What replaced HCPCS code K0554?

E2103 replaced K0554 as the receiver code for a non-adjunctive CGM. Its monthly supplies bill under A4239. An adjunctive CGM uses E2102 for the receiver and A4238 for supplies.

Was K0553 the adjunctive version of K0554?

No. K0553 was the monthly supply allowance for a therapeutic CGM, while K0554 was its receiver. Both were deleted on December 31, 2022, and K0553 was cross-walked to A4239.

What are the Medicare coverage criteria for a CGM?

Under LCD L33822, the patient must have diabetes and be trained on the CGM. The device must be used per its FDA indications. The patient must be insulin-treated or have problematic hypoglycemia, with a qualifying practitioner visit in the six months before ordering.

Is prior authorization required for a CGM under Medicare?

No. Medicare applies no prior authorization to E2102, E2103, A4238, or A4239. Commercial and Medicare Advantage plans may set their own requirements, so check each payer before delivery.

Which modifiers apply to E2103 and A4239?

Every line carries KX if the patient is insulin-treated, or KS if not, never both. Add CG when all five LCD criteria are met. Add KF only when the CGM is an FDA Class III device. On E2102 and A4238, KF is required on every line.

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