FDA product code · Clinical toxicology

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Name: FDA decisions, review times, recalls and adverse event reports for product code MIG
Creator: 510(k) Report

MIGClass U2 decisions since 19920 recalls

2 FDA decisions since 1992. No recall names this code.

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 MIG 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 · MIG

FDA has decided no MIG device since 2007.

Median 510(k) review, days · MIG

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

Recalls per year · MIG

No recall names MIG since 2007.

Adverse event reports per year · MIG

2in 2017

2007high 2 (2017) · low 0 (2007)2025

MAUDE reports naming product code MIG, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Median 510(k) review, days	MAUDE reports
2007	—	0
2008	—	0
2009	—	0
2010	—	0
2011	—	0
2012	—	0
2013	—	0
2014	—	0
2015	—	0
2016	—	0
2017	—	2
2018	—	0
2019	—	0
2020	—	0
2021	—	0
2022	—	0
2023	—	0
2024	—	0
2025	—	0
2026	—	—

FIG. 1 — MIG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MIG? 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

Strip, Test Isoniazid

Which MIG devices have the deepest lineage?

What has FDA decided in MIG lately?