510(k) Report

FDA applicant

The RX Rocker Corp.

Newbury Park, CA3 decisions1990–19900 recalls

FDA records 3 decisions for The RX Rocker Corp. (Newbury Park, CA) in 1990: 3 510(k) clearances. All are in product code IOR (Wheelchair, Mechanical). 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 The RX Rocker Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The RX Rocker Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The RX Rocker Corp. 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?

  • IORWheelchair, Mechanical3decisions

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K902438RX Rocker WheelchairThe RX Rocker Corp. · 19901cites it

What has FDA decided for it lately?

  • K902439RX Rocker Triumph WheelchairThe RX Rocker Corp. · 1990
  • K902438RX Rocker WheelchairThe RX Rocker Corp. · 1990
  • K902440RX Rocker Triumph, JR. WheelchairThe RX Rocker Corp. · 1990

All 3 as The RX Rocker Corp. →