FDA applicant

Allied Healthcare Products, Inc.

Saint Louis, MO26 decisions1981–20140 recalls

FDA records 26 decisions for Allied Healthcare Products, Inc. (Saint Louis, MO) from 1981 to 2014: 26 510(k) clearances. Most are in product codes BTL (Ventilator, Emergency, Powered (Resuscitator)) and BTM (Ventilator, Emergency, Manual (Resuscitator)). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided Allied Healthcare Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2014

2007high 3 (2008) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Allied Healthcare Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Allied”

FDA records each applicant name separately; these may or may not be the same firm.

Allied Associates, Inc. 9 Allied Biomedical Corp. 9 Allied Instrumentation Laboratory 7 Allied Signal, Inc. 2 Allied Rubber Industries Sdn. Bhd. 2 Allied Photo Products Co., Inc. 1 Allied Hill Enterprises, Ltd. 1 Allied Dental Solutions 1 Allied Medical Technologies, Inc. 1 Allied Fisher Scientific 1 Allied Systems Co. 1 Allied Advanced Technologies (Aat) 1

Allied Healthcare Products, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Allied”