# Canadian Bioclinical, Ltd.

- Location (FDA's records): Ontario Mix 1b4, CA
- FDA decisions: 4 (1987–1994): 4 510(k) clearances
- Product codes: DPO (1), CGR (1), LCX (1), CDP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K933794: Ani Biocard (TM) HCG Test (May 19, 1994)
- K870969: Cortisol-Ria Kit Coated Tube Radioimmunoassay Kit (Jun 22, 1987)
- K870968: Total T3-Ria Kit Coated Tube Radioimmunoassay Kit (Jun 22, 1987)
- K864449: Digoxin/Ria Kit Coated Tube Radioimmunoassay Kit (Feb 2, 1987)

Source page: https://510kreport.com/company/canadian-bioclinical