FDA applicant

American Health Products, Inc.

North Brook, IL5 decisions1988–19980 recalls

FDA records 5 decisions for American Health Products, Inc. (North Brook, IL) from 1988 to 1998: 5 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for American Health Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like American Health 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

American Health Products, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?