A.C. POWER PATIENT LIFT— 510(k) K935351

Substantially Equivalent

Ken Kemmerer

FDA 510(k) clearance K935351 for A.C. POWER PATIENT LIFT, Substantially Equivalent on 1994-02-28. Applicant: Ken Kemmerer.

Clearance details

Applicant: Ken Kemmerer
Product code: Code FNG
Advisory panel: General Hospital
Date received: 1993-11-05
Decision date: 1994-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilkes Barre Twp, PA, US

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Adverse events under product code FNG

product code FNG

Death: 4
Total: 4

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.