Canadian Bioclinical, Ltd.
Ontario Mix 1b4, CA
Canadian Bioclinical, Ltd. appears in FDA device records in Ontario Mix 1b4, CA. FDA records list 4 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 4
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 4 510(k) clearances for Canadian Bioclinical, Ltd. between 1987 and 1994. The busiest year on record is 1987, with 3. The most recent is 1994, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1987 | 3 |
| 1994 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K933794 | ANI BIOCARD(TM) HCG TEST | LCX | Substantially Equivalent | |
| K870969 | CORTISOL-RIA KIT COATED TUBE RADIOIMMUNOASSAY KIT | CGR | Substantially Equivalent | |
| K870968 | TOTAL T3-RIA KIT COATED TUBE RADIOIMMUNOASSAY KIT | CDP | Substantially Equivalent | |
| K864449 | DIGOXIN/RIA KIT COATED TUBE RADIOIMMUNOASSAY KIT | DPO | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain