510(k) Report

FDA applicant

Ken Kemmerer

Wilkes Barre Twp, PA2 decisions1994–19960 recalls

FDA records 2 decisions for Ken Kemmerer (Wilkes Barre Twp, PA) from 1994 to 1996: 2 510(k) clearances. Most are in product codes FNG (Lift, Patient, Ac-Powered) and INO (Chair, Positioning, Electric). 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, general hospital panel, where it files most

How often FDA has decided Ken Kemmerer’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ken Kemmerer since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • FNGLift, Patient, Ac-Powered1decision
  • INOChair, Positioning, Electric1decision

What has FDA decided for it lately?

  • K961663Electric Seat Lift ChairKen Kemmerer · 1996
  • K935351A.C. Power Patient LiftKen Kemmerer · 1994

All 2 as Ken Kemmerer →