FDA applicant

Electromek Diagnostic Systems, Inc.

Troy, IL11 decisions1990–19910 recalls

FDA records 11 decisions for Electromek Diagnostic Systems, Inc. (Troy, IL) from 1990 to 1991: 11 510(k) clearances. Most are in product codes IZO (Generator, High-Voltage, X-Ray, Diagnostic) and JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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, radiology panel, where it files most

How often FDA has decided Electromek Diagnostic Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Electromek Diagnostic Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Electromek Diagnostic Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?