FDA applicant

Medimatic

Mchenry, IL5 decisions1978–19870 recalls

FDA records 5 decisions for Medimatic (Mchenry, IL) from 1978 to 1987: 5 510(k) clearances. Most are in product codes IZD (Probe, Uptake, Nuclear) and JOM (Plethysmograph, Photoelectric, Pneumatic Or…). 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 Medimatic’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medimatic since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medimatic

Which product codes does it file in?

What has FDA decided for it lately?