Cambridge Bioscience Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cambridge Bioscience Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Cambridge Bioscience Corp. has 5 FDA 510(k) cleared medical devices. Based in Hopkinton, US.
Historical record: 5 cleared submissions from 1985 to 1989. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Cambridge Bioscience Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cambridge Bioscience Corp.
5 devices
Cleared
Mar 15, 1989
HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES
Microbiology
57d
Cleared
Jul 08, 1988
ADENOCLONE(R)-TYPE 40/41 EIA DIAGNOSTIC TEST (48)
Microbiology
64d
Cleared
Feb 24, 1988
ADENOCLONE(TM)-EIA ADENOVIRUS ANTIGEN TEST
Microbiology
203d
Cleared
Feb 24, 1988
ADENOCLONE(TM)-IFA, ADENOVIRUS ANTIGEN TEST
Microbiology
190d
Cleared
Nov 05, 1985
ROTACLONE ROTAVIRUS DIAGNOSTIC KIT
Microbiology
113d