510(k) Report

FDA applicant

Epm Information Systems, Inc.

Midlothian, VA4 decisions1990–19940 recalls

FDA records 4 decisions for Epm Information Systems, Inc. (Midlothian, VA) from 1990 to 1994: 4 510(k) clearances. Most are in product codes BZQ (Monitor, Breathing Frequency) and LXJ (Interactive Rehabilitation Exercise Devices). 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 Information Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Epm Information Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Epm Information Systems, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Epm Information Systems, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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