510(k) Report

FDA product code · Anesthesiology

Calculator, Pulmonary Function Data

BZCClass II21 CFR 868.1880510(k) required90 decisions since 19773 recalls

90 FDA decisions since 1977. 510(k) reviews decided 2021–2025 took a median of 229 days (half between 229 and 229). 3 recalls name this code, 0 of them Class I. The most-cited predicate is K150810, 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 BZC 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 · BZC

1in 2024

2007: 12011: 12014: 22015: 12016: 12017: 12018: 12019: 22024: 1
2007high 2 (2014) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BZC

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

Recalls per year · BZC

3in 2009

2009: 3
2007high 3 (2009) · low 0 (2007)2026

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

Adverse event reports per year · BZC

3in 2025

2007: 12008: 32016: 42017: 12018: 12019: 72020: 32021: 52022: 92023: 82024: 82025: 3
2007high 9 (2022) · low 0 (2009)2025

MAUDE reports naming product code BZC, 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
20071—01
20080—03
20090—30
20100—00
20111—00
20120—00
20130—00
20142—00
20151—00
20161—04
20171—01
20181—01
20192—07
20200—03
20210—05
20220—09
20230—08
20241—08
20250—03
20260—0—
FIG. 1 — BZC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in BZC? 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