510(k) Report

FDA product code · Hematology

Warmer, Blood, Non-Electromagnetic Radiation

BSBClass II21 CFR 864.9205510(k) required14 decisions since 19761 recall

14 FDA decisions since 1976. 1 recall names this code; it is not Class I. The most-cited predicate is K973741, named by 7 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, hematology panel

Twenty years of BSB 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 · BSB

1in 2011

2009: 12011: 1
2007high 1 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BSB

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

Recalls per year · BSB

1in 2014

2014: 1
2007high 1 (2014) · low 0 (2007)2026

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

Adverse event reports per year · BSB

197in 2025

2007: 42008: 52010: 62011: 352012: 42013: 52014: 102015: 112016: 662017: 292018: 362019: 1472020: 2162021: 3402022: 4472023: 2902024: 2822025: 197
2007high 447 (2022) · low 0 (2009)2025

MAUDE reports naming product code BSB, 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—04
20080—05
20091—00
20100—06
20111—035
20120—04
20130—05
20140—110
20150—011
20160—066
20170—029
20180—036
20190—0147
20200—0216
20210—0340
20220—0447
20230—0290
20240—0282
20250—0197
20260—0—
FIG. 1 — BSB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in BSB? 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 864.9205.