510(k) Report

FDA applicant

Epm Development Systems Corp.

Midlothian, VA1 decision1994–19940 recalls

FDA records 1 decision for Epm Development Systems Corp. (Midlothian, VA) in 1994: 1 510(k) clearance. All are in product code BZQ (Monitor, Breathing Frequency). 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 Epm Development Systems Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Epm Development Systems Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Epm Development Systems 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?

  • BZQMonitor, Breathing Frequency1decision

Who builds on its devices?

Later devices cite its devices 2 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.

  • K941759Snoring SensorEpm Development Systems Corp. · 19942cite it

What has FDA decided for it lately?

  • K941759Snoring SensorEpm Development Systems Corp. · 1994

The one decision as Epm Development Systems Corp. →