510(k) Report

FDA product code · Clinical toxicology

Enzyme Immunoassay, Valproic Acid

LEGClass II21 CFR 862.3645510(k) required35 decisions since 19807 recalls

35 FDA decisions since 1980. 7 recalls name this code, 0 of them Class I. The most-cited predicate is K042476, 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 toxicology panel

Twenty years of LEG 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 · LEG

1in 2009

2009: 1
2007high 1 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LEG

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

Recalls per year · LEG

1in 2018

2007: 12011: 12018: 1
2007high 1 (2007) · low 0 (2008)2026

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

Adverse event reports per year · LEG

5in 2025

2007: 122008: 382009: 182010: 132011: 382012: 292013: 292014: 202015: 32016: 252017: 82018: 242019: 132020: 92021: 122022: 192023: 12024: 142025: 5
2007high 38 (2008) · low 1 (2023)2025

MAUDE reports naming product code LEG, 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—112
20080—038
20091—018
20100—013
20110—138
20120—029
20130—029
20140—020
20150—03
20160—025
20170—08
20180—124
20190—013
20200—09
20210—012
20220—019
20230—01
20240—014
20250—05
20260—0—
FIG. 1 — LEG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in LEG? 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.