FDA applicant

Life Support Products, Inc.

Irvine, CA20 decisions1985–19950 recalls

FDA records 20 decisions for Life Support Products, Inc. (Irvine, CA) from 1985 to 1995: 20 510(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 Life Support Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Life Support Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Life Support Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?