510(k) Report

FDA product code · Anesthesiology

Filter, Conduction, Anesthetic

BSNClass II21 CFR 868.5130510(k) required9 decisions since 19781 recall

9 FDA decisions since 1978. 1 recall names this code; it is not Class I. The most-cited predicate is K083451, 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, anesthesiology panel

Twenty years of BSN 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 · BSN

1in 2019

2009: 12014: 12019: 1
2007high 1 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BSN

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

Recalls per year · BSN

1in 2009

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

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

Adverse event reports per year · BSN

6in 2025

2011: 22012: 882013: 12018: 12019: 12020: 12021: 32022: 232023: 182024: 112025: 6
2007high 88 (2012) · low 0 (2007)2025

MAUDE reports naming product code BSN, 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
20091—10
20100—00
20110—02
20120—088
20130—01
20141—00
20150—00
20160—00
20170—00
20180—01
20191—01
20200—01
20210—03
20220—023
20230—018
20240—011
20250—06
20260—0—
FIG. 1 — BSN by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in BSN? 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