FDA applicant
Life Corp.
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
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.
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