FDA applicant

Eaton Medical Group

Eaton, MI15 decisions1983–19860 recalls

FDA records 15 decisions for Eaton Medical Group (Eaton, MI) from 1983 to 1986: 15 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and DSF (Recorder, Paper Chart). 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, cardiovascular panel, where it files most

How often FDA has decided Eaton Medical Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eaton Medical Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Eaton Medical Group by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Eaton”

FDA records each applicant name separately; these may or may not be the same firm.

Eaton Medical Corp. 5

Eaton Medical Group

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Eaton”