Dako Diagnostics , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Dako Diagnostics , Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Dako Diagnostics , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Cambridgeshire, GB.
Historical record: 6 cleared submissions from 1993 to 1998. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Dako Diagnostics , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dako Diagnostics , Ltd.
6 devices
Cleared
Sep 28, 1998
IMAGEARAINFLUENZA VIRUS GROUP (TYPES 1,2 AND 3) TEST AND IMAGEN PARAINFLUENZA...
Microbiology
188d
Cleared
Dec 22, 1997
IMAGEN RESPIRATORY SCREEN
Microbiology
74d
Cleared
Dec 26, 1996
IMAGEN RESPIRATORY SCREEN
Microbiology
216d
Cleared
Jan 11, 1996
IDEIA(TM) CHLAMYDIA BLOCKING REAGENTS, MODIFICATION
Microbiology
707d
Cleared
Jan 09, 1995
IMAGEN
Microbiology
171d
Cleared
Dec 27, 1993
IDEIA(TM) ROTAVIRUS
Microbiology
224d