FDA applicant
Clinical Bioresearch
FDA records 4 decisions for Clinical Bioresearch (Mchenry, IL) in 1978: 4 510(k) clearances. Most are in product codes CDP (Radioimmunoassay, Total Triiodothyronine) and CDX (Radioimmunoassay, Total Thyroxine). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Clinical Bioresearch’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Clinical Bioresearch since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Clinical Bioresearch’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report