510(k) Report

FDA applicant

Ria Products, Inc.

Mchenry, IL9 decisions1978–19810 recalls

FDA records 9 decisions for Ria Products, Inc. (Mchenry, IL) from 1978 to 1981: 9 510(k) clearances. Most are in product codes CDD (Radioassay, Vitamin B12) and CGN (Acid, Folic, Radioimmunoassay). 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 Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ria Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ria Products, Inc.’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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