Columbia Bioscience, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Columbia Bioscience, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Columbia Bioscience, Inc. has 13 FDA 510(k) cleared medical devices. Based in Frederick, US.
Historical record: 13 cleared submissions from 1996 to 1999. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Columbia Bioscience, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Columbia Bioscience, Inc.
13 devices
Cleared
Sep 03, 1999
IS H. PYLORI IGG ELISA TEST SYSTEM
Microbiology
203d
Cleared
Sep 03, 1999
MUMPS IGG ELISA TEST SYSTEM
Microbiology
143d
Cleared
Feb 02, 1999
IS ANTI-TPO IGG ELISA TEST SYSTEM
Immunology
69d
Cleared
Dec 16, 1998
IS BORRELIA BURGDORFERI IGG/IGM ELISA TEST SYSTEM
Microbiology
63d
Cleared
Dec 16, 1998
IS BORRELIA BURGDORFERI IGM TEST SYSTEM
Microbiology
63d
Cleared
Dec 07, 1998
ANTI-TG IGG ELISA TEST SYSTEM
Immunology
59d
Cleared
Nov 25, 1998
EBNA-1 IGM ELISA TEST SYSTEM
Microbiology
142d
Cleared
Nov 25, 1998
EA-D IGM ELISA TEST SYSTEM
Microbiology
142d
Cleared
Nov 25, 1998
VCA IGM ELISA TEST SYSTEM
Microbiology
142d
Cleared
Nov 18, 1998
IS-ANTI-MPO IGG ELISA TEST SYSTEM
Immunology
54d
Cleared
Nov 18, 1998
IS-ANTI-PR3 IGG ELISA TEST SYSTEM
Immunology
27d
Cleared
Nov 05, 1996
ANTHOS PHACTS VERSION MICROPLATE READER
Chemistry
158d
Cleared
Aug 02, 1996
CBI 7520 READER
Chemistry
129d