510(k) Report

FDA applicant

Medical Diagnostics, Ca.

Mchenry, IL4 decisions1983–19860 recalls

FDA records 4 decisions for Medical Diagnostics, Ca. (Mchenry, IL) from 1983 to 1986: 4 510(k) clearances. Most are in product codes DBM (Antimitochondrial Antibody, Indirect…) and DNK (Thin Layer Chromatography, Morphine). 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, immunology panel, where it files most

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

FDA decisions per year

No FDA decision for Medical Diagnostics, Ca. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medical Diagnostics, Ca.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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