510(k) Report

FDA applicant

Altoona Medical Supply

Altoona, IA3 decisions1989–19920 recalls

FDA records 3 decisions for Altoona Medical Supply (Altoona, IA) from 1989 to 1992: 3 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and GZQ (Instrument, Dowel Cutting). 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 Altoona Medical Supply’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Altoona Medical Supply since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Altoona Medical Supply 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?

  • IPFStimulator, Muscle, Powered1decision
  • GZQInstrument, Dowel Cutting1decision
  • ILZAccessories, Traction1decision

Who builds on its devices?

Later devices cite its devices 7 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.

  • K893874Fujitens IiiAltoona Medical Supply · 19895cite it
  • K913272EMS/400Altoona Medical Supply · 19912cite it

What has FDA decided for it lately?

  • K921711Flexion Distration SupportAltoona Medical Supply · 1992
  • K913272EMS/400Altoona Medical Supply · 1991
  • K893874Fujitens IiiAltoona Medical Supply · 1989

All 3 as Altoona Medical Supply →