510(k) Report

FDA applicant

W. Murphy Ent., Inc.

Ontario, CA3 decisions1990–19910 recalls

FDA records 3 decisions for W. Murphy Ent., Inc. (Ontario, CA) from 1990 to 1991: 3 510(k) clearances. All are in product code FPP (Stretcher, Hand-Carried). 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 W. Murphy Ent., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for W. Murphy Ent., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — W. Murphy Ent., 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?

  • FPPStretcher, Hand-Carried3decisions

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.

  • K902521Weevac 6 Infant Evacuation StretcherW. Murphy Ent., Inc. · 19901cites it

What has FDA decided for it lately?

  • K910709Weevac TC Hand Carried Rescue StretcherW. Murphy Ent., Inc. · 1991
  • K902474Weevac 1 Portable Rescue StretcherW. Murphy Ent., Inc. · 1990
  • K902521Weevac 6 Infant Evacuation StretcherW. Murphy Ent., Inc. · 1990

All 3 as W. Murphy Ent., Inc. →