FDA applicant

Life Products, Inc.

Boulder, CO10 decisions1977–19900 recalls

FDA records 10 decisions for Life Products, Inc. (Boulder, CO) from 1977 to 1990: 10 510(k) clearances. Most are in product codes CBK (Ventilator, Continuous, Facility Use) and BZO (Set, Tubing And Support, Ventilator (W Harness)). 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 Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Life Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?