510(k) Report

FDA product code · Clinical toxicology

Kit, Test, Multiple, Drugs Of Abuse, Over The Counter

MVOClass U510(k) required18 decisions since 19981 recall

18 FDA decisions since 1998. 1 recall names this code; it is not Class I. The most-cited predicate is K003858, 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 MVO 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 · MVO

FDA has decided no MVO device since 2007.

Median 510(k) review, days · MVO

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

Recalls per year · MVO

1so far in 2026, the most since 2007

2026 (partial year): 1
2007high 1 (2026) · low 0 (2007)2026

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

Adverse event reports per year · MVO

1in 2015

2007: 12008: 12009: 22013: 32015: 1
2007high 3 (2013) · low 0 (2010)2025

MAUDE reports naming product code MVO, 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—01
20080—01
20090—02
20100—00
20110—00
20120—00
20130—03
20140—00
20150—01
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—1—
FIG. 1 — MVO by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MVO? 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