510(k) Report

FDA product code · Clinical toxicology

Nad-Nadh, Specific Reagent For Alcohol Enzyme Method

DMLClass II21 CFR 862.3040510(k) required13 decisions since 19841 recall

13 FDA decisions since 1984. 1 recall names this code; it is not Class I. The most-cited predicate is K993980, 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 DML 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 · DML

FDA has decided no DML device since 2007.

Median 510(k) review, days · DML

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

Recalls per year · DML

No recall names DML since 2007.

Adverse event reports per year · DML

2in 2024

2011: 22018: 12020: 12021: 12022: 12023: 22024: 2
2007high 2 (2011) · low 0 (2007)2025

MAUDE reports naming product code DML, 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—02
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—01
20190—00
20200—01
20210—01
20220—01
20230—02
20240—02
20250—00
20260—0—
FIG. 1 — DML by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in DML? 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 862.3040.