Cozart Bioscience , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Cozart Bioscience , Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Cozart Bioscience , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Oxfordshire Ox14 4ru, GB.
Historical record: 6 cleared submissions from 2001 to 2004. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Cozart Bioscience , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cozart Bioscience , Ltd.
6 devices
Cleared
Jun 03, 2004
COZART EIA AMPHETAMINES ORAL FLUID MICROPLATE KIT
Toxicology
188d
Cleared
May 14, 2003
COZART EIA COTININE URINE KIT
Toxicology
335d
Cleared
Apr 28, 2003
COZART EIA COCAINE ORAL FLIUD KIT
Toxicology
95d
Cleared
Apr 07, 2003
COZART EIA OPIATES ORAL FLUID KIT
Toxicology
101d
Cleared
Nov 05, 2002
COZART RAPISCAN ORAL FLUID DRUG TEST - OPIATE/METHADONE
Toxicology
229d
Cleared
Jul 31, 2001
METHADONE MICROPLATE EIA URINE APPLICATION
Toxicology
109d