510(k) Report

FDA applicant

Quickie Designs, Inc.

Fresno, CA6 decisions1990–19970 recalls

FDA records 6 decisions for Quickie Designs, Inc. (Fresno, CA) from 1990 to 1997: 6 510(k) clearances. All are in product code ITI (Wheelchair, Powered). 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 Quickie Designs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Quickie Designs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Quickie Designs, Inc. 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, Powered6decisions

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K924278Quickie P200Quickie Designs, Inc. · 19942cite it
  • K900330Quickie P300 WheelchairQuickie Designs, Inc. · 19901cites it

What has FDA decided for it lately?

  • K972230Quickie P90 SeriesQuickie Designs, Inc. · 1997
  • K963382Quickie P100 SeriesQuickie Designs, Inc. · 1997
  • K963381Quickie P300 SeriesQuickie Designs, Inc. · 1997
  • K963385Quickie Power Wheelchairs P200 SeriesQuickie Designs, Inc. · 1997
  • K924278Quickie P200Quickie Designs, Inc. · 1994
  • K900330Quickie P300 WheelchairQuickie Designs, Inc. · 1990

All 6 as Quickie Designs, Inc. →