FDA applicant

Ria Diagnostics

Mchenry, IL7 decisions1978–19860 recalls

FDA records 7 decisions for Ria Diagnostics (Mchenry, IL) from 1978 to 1986: 7 510(k) clearances. Most are in product codes CDP (Radioimmunoassay, Total Triiodothyronine) and DON (Radioimmunoassay, Digoxin (125-I), Rabbit…). 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 Ria Diagnostics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ria Diagnostics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ria Diagnostics

Which product codes does it file in?

What has FDA decided for it lately?