510(k) Report

FDA product code · Clinical chemistry

Bilirubin (Total And Unbound) In The Neonate Test System

MQMClass I21 CFR 862.1113510(k) required17 decisions since 19920 recalls

17 FDA decisions since 1992. No recall names this code. The most-cited predicate is K922770, 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 chemistry panel

Twenty years of MQM 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 · MQM

1in 2017

2008: 12011: 12014: 22017: 1
2007high 2 (2014) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQM

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

Recalls per year · MQM

No recall names MQM since 2007.

Adverse event reports per year · MQM

2in 2025

2007: 52008: 32010: 42011: 32012: 42014: 12015: 12016: 12017: 12018: 52019: 62020: 12021: 12023: 142024: 172025: 2
2007high 17 (2024) · low 0 (2009)2025

MAUDE reports naming product code MQM, 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—05
20081—03
20090—00
20100—04
20111—03
20120—04
20130—00
20142—01
20150—01
20160—01
20171—01
20180—05
20190—06
20200—01
20210—01
20220—00
20230—014
20240—017
20250—02
20260—0—
FIG. 1 — MQM by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MQM? 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