510(k) Report

FDA product code · Clinical chemistry

Differential Rate Kinetic Method, Cpk Or Isoenzymes

JHSClass II21 CFR 862.1215510(k) required38 decisions since 19788 recalls

38 FDA decisions since 1978. 8 recalls name this code, 0 of them Class I. The most-cited predicate is K062128, named by 1 later device.

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 JHS 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 · JHS

1in 2016

2008: 12011: 12016: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JHS

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

Recalls per year · JHS

1in 2020

2013: 22018: 52020: 1
2007high 5 (2018) · low 0 (2007)2026

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

Adverse event reports per year · JHS

10in 2025

2008: 52009: 112010: 262011: 182012: 12013: 22014: 32015: 32016: 12017: 12018: 62019: 62020: 132021: 42022: 32023: 122024: 142025: 10
2007high 26 (2010) · low 0 (2007)2025

MAUDE reports naming product code JHS, 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
20070—00
20081—05
20090—011
20100—026
20111—018
20120—01
20130—22
20140—03
20150—03
20161—01
20170—01
20180—56
20190—06
20200—113
20210—04
20220—03
20230—012
20240—014
20250—010
20260—0—
FIG. 1 — JHS by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in JHS? 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.