510(k) Report

FDA product code · Clinical chemistry

Colorimetric Method, Cpk Or Isoenzymes

JHYClass II21 CFR 862.1215510(k) required40 decisions since 19761 recall

40 FDA decisions since 1976. 1 recall names this code; it is not Class I. The most-cited predicate is K970343, named by 3 later devices.

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

FIG. A — Illustration, clinical chemistry panel

Twenty years of JHY at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · JHY

1in 2015

2007: 12013: 12014: 22015: 1
2007high 2 (2014) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JHY

Too few JHY 510(k)s in any year since 2007 to give a median.

Recalls per year · JHY

1in 2010

2010: 1
2007high 1 (2010) · low 0 (2007)2026

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

Adverse event reports per year · JHY

3in 2023

2012: 12014: 32015: 22016: 42017: 112018: 52019: 22020: 22022: 12023: 3
2007high 11 (2017) · low 0 (2007)2025

MAUDE reports naming product code JHY, 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
20071—00
20080—00
20090—00
20100—10
20110—00
20120—01
20131—00
20142—03
20151—02
20160—04
20170—011
20180—05
20190—02
20200—02
20210—00
20220—01
20230—03
20240—00
20250—00
20260—0—
FIG. 1 — JHY by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in JHY? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 862.1215.