510(k) Report

510(k) · Cleared

Cleared

Genchem Creatinine Reagent

K040976510(k) TraditionalCleared Dec 27, 2004257-day reviewClass II21 CFR 862.1225

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Genchem, Inc. · CGX Alkaline Picrate, Colorimetry, Creatinine

Cleared on Dec 27, 2004 as substantially equivalent to K915077 (Beckman Instruments, Inc., 1991) after a 257-day review. Its family tree reaches back 1 generation to 1991.

Decided
Dec 27, 2004
Review
257 days
Class
Class II
Product code
CGX
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K915077 (1991). No later device cites it as a predicate yet.

K915077 · Synchron Creatinine Triggered Test CX4,5,7, · Beckman Instruments, Inc. · 19911990199520002005
  1. Root · 1 generation backK915077 Synchron Creatinine Triggered Test CX4,5,7,Beckman Instruments, Inc. · 1991
  2. This deviceK040976 Genchem Creatinine ReagentGenchem, Inc. · 2004
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K915077Synchron Creatinine Triggered Test CX4,5,7,Beckman Instruments, Inc.1991—
0 (this device)K040976Genchem Creatinine ReagentGenchem, Inc.2004—
FIG. 1 — Lineage of K040976, 1991–2004Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in CGX? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new CGX device

  1. #1 K242685 Atellica® CH Creatinine_3 (Crea3)score 12.1 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K915077Synchron Creatinine Triggered Test CX4,5,7,
Summary page 1
…CX3® System. 5.0 Substantial Equivalence Information: a. Predicate Device Name: Beckman Creatinine Reagent for the CX3 b. Predicate K Number: K915077 c. Comparison with Predicate: Both Reagents are similar in design, function and chemical principle as well as ingr…
Beckman Instruments, Inc.1991—

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Its one ancestor has no recall.

How does its category compare?

All CGX devices

CGX Alkaline Picrate, Colorimetry, Creatinine: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CGX

1in 2025

2007: 42009: 12012: 12013: 12014: 22016: 12022: 12024: 22025: 12026 (partial year): 1
2007high 4 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CGX

25in 2007

2007: 25 days median
2007high 25 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · CGX

2in 2016

2008: 12009: 22010: 22011: 12012: 22016: 22026 (partial year): 1
2007high 2 (2009) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · CGX

34in 2025

2007: 152008: 272009: 52010: 52011: 322012: 132013: 242014: 132015: 132016: 32017: 212018: 142019: 252020: 192021: 132022: 232023: 192024: 322025: 34
2007high 34 (2025) · low 3 (2016)2025

MAUDE reports naming product code CGX, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007425015
20080—127
20091—25
20100—25
20110—132
20121—213
20131—024
20142—013
20150—013
20161—23
20170—021
20180—014
20190—025
20200—019
20210—013
20221—023
20230—019
20242—032
20251—034
20261—1—

What is it indicated for?

The GenChem Creatinine Test Reagent System is intended for the quantitative determination of creatinine in serum, plasma and urine on the Beckman SYNCHRON CX3® System and as an aid in the diagnosis of renal impairment and diseases such as chronic glomerulonephritis, diabetic nephropathy, chronic interstitial nephritis and as an indicator of glomerular filtration rate.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K040976: Genchem Creatinine Reagent.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K040976

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026