510(k) Report

FDA product code · Clinical toxicology

Enzyme Immunoassay, Carbamazepine

KLTClass II21 CFR 862.3645510(k) required56 decisions since 19784 recalls

56 FDA decisions since 1978. 4 recalls name this code, 0 of them Class I. The most-cited predicate is K955100, 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 toxicology panel

Twenty years of KLT 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 · KLT

1in 2015

2007: 12011: 12013: 12015: 1
2007high 1 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KLT

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

Recalls per year · KLT

1in 2013

2013: 1
2007high 1 (2013) · low 0 (2007)2026

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

Adverse event reports per year · KLT

4in 2025

2009: 22010: 12011: 12012: 12013: 12014: 32015: 92016: 32017: 12018: 42019: 62020: 12021: 22022: 72023: 32024: 12025: 4
2007high 9 (2015) · low 0 (2007)2025

MAUDE reports naming product code KLT, 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—02
20100—01
20111—01
20120—01
20131—11
20140—03
20151—09
20160—03
20170—01
20180—04
20190—06
20200—01
20210—02
20220—07
20230—03
20240—01
20250—04
20260—0—
FIG. 1 — KLT by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in KLT? 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 862.3645.