Alfa Biotech (Uk) , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Alfa Biotech (Uk) , Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Alfa Biotech (Uk) , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Aldershot, GB.
Historical record: 3 cleared submissions from 1998 to 1998. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Alfa Biotech (Uk) , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alfa Biotech (Uk) , Ltd.
3 devices
Cleared
Mar 24, 1998
AURAFLEX TSH-3 200 TEST PACK MODEL NUMBER 80600, AURAFLEX TSH-3 CALIBRATOR...
Chemistry
35d
Cleared
Feb 17, 1998
AURAFLEX FERRITIN 200 TEST PACK 80500, AURAFLEX FERRITIN CALIBRATOR PACK 80501
Immunology
78d
Cleared
Feb 02, 1998
AURAFLEX FT3 150 TEST PACK, AURAFLEX FT3 CALIBRATOR PACK
Chemistry
102d