FDA applicant

American Life Support Technology, Inc.

Redwood City, CA1 decision1994–19940 recalls

FDA records 1 decision for American Life Support Technology, Inc. (Redwood City, CA) in 1994: 1 510(k) clearance. All are in product code INX (Bed, Air Fluidized). 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, physical medicine panel, where it files most

How often FDA has decided American Life Support Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Life Support Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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American Life Support Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?