Cozart Bioscience, Ltd.
Oxfordshire Ox14 4ru, GB
Cozart Bioscience , Ltd. appears in FDA device records in Oxfordshire Ox14 4ru, GB. FDA records list 6 510(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
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Cozart Bioscience, Ltd. between 2001 and 2004. The busiest year on record is 2003, with 3. The most recent is 2004, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2001 | 1 |
| 2002 | 1 |
| 2003 | 3 |
| 2004 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K033743 | COZART EIA AMPHETAMINES ORAL FLUID MICROPLATE KIT | DKZ | Substantially Equivalent | |
| K021944 | COZART EIA COTININE URINE KIT | MKU | Substantially Equivalent | |
| K030234 | COZART EIA COCAINE ORAL FLIUD KIT | DIO | Substantially Equivalent | |
| K024339 | COZART EIA OPIATES ORAL FLUID KIT | DIG | Substantially Equivalent | |
| K020920 | COZART RAPISCAN ORAL FLUID DRUG TEST - OPIATE/METHADONE | DJG | Substantially Equivalent | |
| K011131 | METHADONE MICROPLATE EIA URINE APPLICATION | DJR | 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