510(k) Report

FDA product code · Immunology

System, Test, Thyroglobulin

MSWClass II21 CFR 866.6010510(k) required13 decisions since 19994 recalls

13 FDA decisions since 1999. 510(k) reviews decided 2021–2025 took a median of 267 days (half between 85 and 458). 4 recalls name this code, 0 of them Class I. The most-cited predicate is K002905, 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, immunology panel

Twenty years of MSW 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 · MSW

1in 2025

2023: 22024: 22025: 1
2007high 2 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MSW

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

Recalls per year · MSW

1in 2023

2010: 12022: 22023: 1
2007high 2 (2022) · low 0 (2007)2026

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

Adverse event reports per year · MSW

3in 2025

2012: 22013: 22015: 12016: 12017: 32018: 52019: 22022: 572023: 42024: 32025: 3
2007high 57 (2022) · low 0 (2007)2025

MAUDE reports naming product code MSW, 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—10
20110—00
20120—02
20130—02
20140—00
20150—01
20160—01
20170—03
20180—05
20190—02
20200—00
20210—00
20220—257
20232—14
20242—03
20251—03
20260—0—
FIG. 1 — MSW by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MSW? 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 866.6010.