Alamar Biosciences, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alamar Biosciences, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Alamar Biosciences, Inc. has 5 FDA 510(k) cleared medical devices. Based in Sacramento, US.
Historical record: 5 cleared submissions from 1993 to 1995. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Alamar Biosciences, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alamar Biosciences, Inc.
5 devices
Cleared
Feb 17, 1995
MICRODILUTION DEVICE FOR DETERMINING GENTAMICIN & STRRPTOMYCIN FOR DETECTION...
Microbiology
199d
Cleared
Oct 21, 1994
ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL MODIFICATION
Microbiology
25d
Cleared
Nov 16, 1993
ALAMAR BIOSCIENCES LABORATORY, INC. ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL
Microbiology
98d
Cleared
Oct 22, 1993
READAR
Microbiology
266d
Cleared
Jul 08, 1993
READAR/SUSCEPTIBILITY, GRAM NEGATIVE PANELS
Microbiology
233d