Cozart Bioscience , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K033743 | COZART EIA AMPHETAMINES ORAL FLUID MICROPLATE KIT | June 3, 2004 |
| K021944 | COZART EIA COTININE URINE KIT | May 14, 2003 |
| K030234 | COZART EIA COCAINE ORAL FLIUD KIT | April 28, 2003 |
| K024339 | COZART EIA OPIATES ORAL FLUID KIT | April 7, 2003 |
| K020920 | COZART RAPISCAN ORAL FLUID DRUG TEST - OPIATE/METHADONE | November 5, 2002 |
| K011131 | METHADONE MICROPLATE EIA URINE APPLICATION | July 31, 2001 |