510(k) Report

FDA product code · Immunology

System,Test,Antibodies,B2 - Glycoprotein I (B2 - Gpi)

MSVClass II21 CFR 866.5660510(k) required46 decisions since 19971 recall

46 FDA decisions since 1997. 1 recall names this code; it is not Class I. The most-cited predicate is K970551, named by 4 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 MSV 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 · MSV

1in 2018

2008: 12009: 12010: 12012: 12015: 22017: 12018: 12026 (partial year): 1
2007high 2 (2015) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MSV

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

Recalls per year · MSV

No recall names MSV since 2007.

Adverse event reports per year · MSV

No MAUDE report names MSV since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20081—00
20091—00
20101—00
20110—00
20121—00
20130—00
20140—00
20152—00
20160—00
20171—00
20181—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20261—0—
FIG. 1 — MSV by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MSV? 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 866.5660.