Company ยท GB
Cozart Bioscience , Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2004. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 3, 2004 | K033743 | COZART EIA AMPHETAMINES ORAL FLUID MICROPLATE KIT Cozart Bioscience , Ltd., GB | DKZ |
| May 14, 2003 | K021944 | COZART EIA COTININE URINE KIT Cozart Bioscience , Ltd., GB | MKU |
| Apr 28, 2003 | K030234 | COZART EIA COCAINE ORAL FLIUD KIT Cozart Bioscience , Ltd., GB | DIO |
| Apr 7, 2003 | K024339 | COZART EIA OPIATES ORAL FLUID KIT Cozart Bioscience , Ltd., GB | DIG |
| Nov 5, 2002 | K020920 | COZART RAPISCAN ORAL FLUID DRUG TEST - OPIATE/METHADONE Cozart Bioscience , Ltd., GB | DJG |
| Jul 31, 2001 | K011131 | METHADONE MICROPLATE EIA URINE APPLICATION Cozart Bioscience , Ltd., GB | DJR |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||