510(k) Report

FDA product code · Clinical toxicology

Colorimetry, Salicylate

DKJClass II21 CFR 862.3830510(k) required29 decisions since 19814 recalls

29 FDA decisions since 1981. 4 recalls name this code, 0 of them Class I. The most-cited predicate is K844070, named by 2 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 toxicology panel

Twenty years of DKJ 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 · DKJ

1in 2010

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

2026 to Oct 25, outlined.

Median 510(k) review, days · DKJ

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

Recalls per year · DKJ

1in 2013

2007: 12013: 1
2007high 1 (2007) · low 0 (2008)2026

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

Adverse event reports per year · DKJ

1in 2020

2007: 12008: 52009: 12011: 32012: 12013: 12020: 1
2007high 5 (2008) · low 0 (2010)2025

MAUDE reports naming product code DKJ, 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—11
20080—05
20090—01
20101—00
20110—03
20120—01
20130—11
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—01
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — DKJ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in DKJ? 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 862.3830.