FDA product code · General hospital

Timer, Apgar

Name: FDA decisions, review times, recalls and adverse event reports for product code LHB
Creator: 510(k) Report

LHBClass I21 CFR 880.2930510(k) exempt2 decisions since 19810 recalls

FDA lists LHB as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 880.9 applies, such as a new intended use or a different fundamental technology. 2 FDA decisions since 1981. No recall names this code.

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, general hospital panel

Twenty years of LHB 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 · LHB

FDA has decided no LHB device since 2007.

Median 510(k) review, days · LHB

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

Recalls per year · LHB

No recall names LHB since 2007.

Adverse event reports per year · LHB

No MAUDE report names LHB since 2007.

View these four charts as a table

Year	Median 510(k) review, days	MAUDE reports
2007	—	0
2008	—	0
2009	—	0
2010	—	0
2011	—	0
2012	—	0
2013	—	0
2014	—	0
2015	—	0
2016	—	0
2017	—	0
2018	—	0
2019	—	0
2020	—	0
2021	—	0
2022	—	0
2023	—	0
2024	—	0
2025	—	0
2026	—	—

FIG. 1 — LHB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in LHB? 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

Timer, Apgar

What has FDA decided in LHB lately?