510(k) Report

FDA product code · Clinical chemistry

Mercuric Thiocyanate, Colorimetry, Chloride

CHJClass II21 CFR 862.1170510(k) required53 decisions since 19770 recalls

53 FDA decisions since 1977. No recall names this code.

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 CHJ 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 · CHJ

FDA has decided no CHJ device since 2007.

Median 510(k) review, days · CHJ

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

Recalls per year · CHJ

No recall names CHJ since 2007.

Adverse event reports per year · CHJ

4in 2020

2020: 4
2007high 4 (2020) · low 0 (2007)2025

MAUDE reports naming product code CHJ, 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
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—04
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — CHJ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in CHJ? 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 862.1170.