FDA applicant

Disa Electronics

Walker, MI2 decisions1982–19820 recalls

FDA records 2 decisions for Disa Electronics (Walker, MI) in 1982: 2 510(k) clearances. Most are in product codes IKN (Electromyograph, Diagnostic) and FAP (Cystometric Gas (Carbon-Dioxide) On Hydraulic…). 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 Disa Electronics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Disa Electronics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Disa”

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

Disa Medinotec 2

Disa Electronics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Disa”