510(k) Report

FDA applicant

Wheelchairs of Kansas

Ellis, KS4 decisions1995–19980 recalls

FDA records 4 decisions for Wheelchairs of Kansas (Ellis, KS) from 1995 to 1998: 4 510(k) clearances. Most are in product codes ITI (Wheelchair, Powered) and FNM (Mattress, Air Flotation, Alternating Pressure). 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, physical medicine panel, where it files most

How often FDA has decided Wheelchairs of Kansas’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wheelchairs of Kansas since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wheelchairs of Kansas 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?

  • ITIWheelchair, Powered2decisions
  • FNMMattress, Air Flotation, Alternating Pressure1decision
  • IORWheelchair, Mechanical1decision

What has FDA decided for it lately?

  • K974319Mighty AirWheelchairs of Kansas · 1998
  • K970743BCW Power Advantage WheelchairWheelchairs of Kansas · 1997
  • K961514BCW Advantage WheelchairWheelchairs of Kansas · 1996
  • K945047BCW 600 Power WheelchairWheelchairs of Kansas · 1995

All 4 as Wheelchairs of Kansas →