FDA applicant

Life Support, Inc.

Mchenry, IL2 decisions1979–19800 recalls

FDA records 2 decisions for Life Support, Inc. (Mchenry, IL) from 1979 to 1980: 2 510(k) clearances. Most are in product codes HFO (Recorder, Pressure, Intrauterine) and HGP (Electrode, Circular (Spiral), Scalp And…). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Life Support, Inc.

Which product codes does it file in?

What has FDA decided for it lately?