510(k) Report

510(k) · Cleared

Cleared

Synchron Creatinine Triggered Test CX4,5,7,

K915077510(k) TraditionalCleared Dec 18, 199140-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

Beckman Instruments, Inc. · CGX Alkaline Picrate, Colorimetry, Creatinine

Cleared on Dec 18, 1991 after a 40-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 1 later device descends from it.

Decided
Dec 18, 1991
Review
40 days
Class
Class II
Product code
CGX
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared1990200020102020
  1. This deviceK915077 Synchron Creatinine Triggered Test CX4,5,7,Beckman Instruments, Inc. · 1991
  2. Descendant · cites it directly · 0 of its ownK040976 Genchem Creatinine ReagentGenchem, Inc. · 2004

Most influential descendants

Showing 1 of 1 · See all
  • K040976Genchem Creatinine ReagentGenchem, Inc. · 2004 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K915077Synchron Creatinine Triggered Test CX4,5,7,Beckman Instruments, Inc.1991—
+1K040976Genchem Creatinine ReagentGenchem, Inc.2004—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
FIG. 1 — Lineage of K915077, 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), 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
Get a 510(k) Report

What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K040976Genchem Creatinine ReagentGenchem, Inc.20040

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?

  • Of its descendants, K040976 (Genchem, Inc., 2004) has gone furthest, with 0 descendants of its own.

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—
Cite this page

510(k) Report. “K915077: Synchron Creatinine Triggered Test CX4,5,7,.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K915077

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026