510(k) Report

FDA applicant

Strom Corp.

Mchenry, IL3 decisions1981–19820 recalls

FDA records 3 decisions for Strom Corp. (Mchenry, IL) from 1981 to 1982: 3 510(k) clearances. All are in product code BYI (Percussor, Powered-Electric). 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, anesthesiology panel, where it files most

How often FDA has decided Strom Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Strom Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Strom 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?

  • BYIPercussor, Powered-Electric3decisions

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.

  • K821570Pneumo Pulssor IiiStrom Corp. · 19821cites it
  • K821265Pneumopulssor (PPS II)Strom Corp. · 19821cites it
  • K813438Pneumo PulssorStrom Corp. · 19811cites it

What has FDA decided for it lately?

  • K821265Pneumopulssor (PPS II)Strom Corp. · 1982
  • K821570Pneumo Pulssor IiiStrom Corp. · 1982
  • K813438Pneumo PulssorStrom Corp. · 1981

All 3 as Strom Corp. →