FDA applicant

Micromedic Systems

Mchenry, IL42 decisions1976–19930 recalls

FDA records 42 decisions for Micromedic Systems (Mchenry, IL) from 1976 to 1993: 42 510(k) clearances. Most are in product codes JLW (Radioimmunoassay, Thyroid-Stimulating Hormone) and JQW (Station, Pipetting And Diluting, For Clinical…). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Micromedic Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Micromedic Systems

Which product codes does it file in?

What has FDA decided for it lately?