510(k) Report

FDA applicant

Life Corp.

Menomonee Falls, WI5 decisions1986–19910 recalls

FDA records 5 decisions for Life Corp. (Menomonee Falls, WI) from 1986 to 1991: 5 510(k) clearances. All are in product code BTL (Ventilator, Emergency, Powered (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 Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Life Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Life Corp.’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