Alamar Biosciences Laboratory, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alamar Biosciences Laboratory, Inc. - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Alamar Biosciences Laboratory, Inc. has 26 FDA 510(k) cleared microbiology devices. Based in Napa, US.
Historical record: 26 cleared submissions from 1989 to 1994.
Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alamar Biosciences Laboratory, Inc.
26 devices
Cleared
Dec 15, 1994
ALAMAR ANTIBIOTIC SUSCEPTIBILITY
Microbiology
267d
Cleared
May 17, 1994
READER
Microbiology
519d
Cleared
Sep 23, 1993
ALAMAR BACTERIAL IDENTIFICATION TEST PANEL
Microbiology
300d
Cleared
Aug 31, 1993
READAR
Microbiology
280d
Cleared
Jun 25, 1993
ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL
Microbiology
148d
Cleared
Apr 05, 1993
ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL
Microbiology
89d
Cleared
Nov 30, 1992
ANTIMICROBIAL SUSCEPTIBILITY TEST
Microbiology
87d
Cleared
Aug 20, 1992
ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL
Microbiology
72d
Cleared
Aug 19, 1992
ANTIMICROBIAL SUSCETIBILITY TEST PANEL
Microbiology
112d
Cleared
Jul 28, 1992
ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL
Microbiology
81d
Cleared
May 15, 1991
ANTIMICROBIAL SUSCEPT. TEST PANEL NITROFURANTOIN
Microbiology
37d
Cleared
Apr 22, 1991
ANTIMICROBIAL AMPICILLIN
Microbiology
35d