Bioclinical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bioclinical Systems, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Bioclinical Systems, Inc. has 13 FDA 510(k) cleared medical devices. Based in St.Louis, US.
Historical record: 13 cleared submissions from 1985 to 1995. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Bioclinical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioclinical Systems, Inc.
13 devices
Cleared
Jun 30, 1995
CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIA
Microbiology
163d
Cleared
Apr 04, 1995
CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGARS
Microbiology
123d
Cleared
Feb 09, 1994
MICROBIOLOGICAL CULTURE MEDIA,MARTIN LEWIS AGAR
Microbiology
229d
Cleared
Feb 03, 1994
MICROBIOLOGICAL CULTURE MEDIA,CHOCOLATE AGAR
Microbiology
223d
Cleared
Aug 24, 1987
ROUND 1
Microbiology
18d
Cleared
Apr 21, 1986
MICRO-ELISA HLH TEST KIT MONOCLONAL
Chemistry
82d
Cleared
Apr 21, 1986
VISI-CHECK HLH TEST MONOCLONAL
Chemistry
82d
Cleared
Apr 11, 1986
MICRO-EIA THEOPHYLLINE TEST KIT MONOCLONAL
Toxicology
102d
Cleared
Jan 13, 1986
MICRO-ELISA HCG EST KIT VISI-CHECK HCG TEST KIT NO
Chemistry
102d
Cleared
Jan 07, 1986
MICRO-ELISA TSH TEST KIT-VISI-CHECK TSH TEST KIT
Chemistry
69d
Cleared
Mar 05, 1985
NOW HOME PREGN. TEST KIT ENZYME IMMUNOASSAY HCG
Chemistry
54d
Cleared
Mar 05, 1985
BCS GLUCOSE COLORIMETRIC TEST
Chemistry
42d