Oxoid , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Oxoid , Ltd. - FDA 510(k) Cleared Devices
36
Total
36
Cleared
0
Denied
Oxoid , Ltd. has 36 FDA 510(k) cleared microbiology devices. Based in Basingstoke, GB.
Historical record: 36 cleared submissions from 1997 to 2007.
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 - Oxoid , Ltd.
36 devices
Cleared
Mar 14, 2007
ERTAPENEM ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
Microbiology
47d
Cleared
Mar 17, 2006
TIGECYCLINE ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
Microbiology
42d
Cleared
Sep 14, 2004
DAPTOMYCIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
Microbiology
35d
Cleared
Apr 02, 2002
OXOID PBP2 1 LATEX AGGLUTINATION TEST
Microbiology
302d
Cleared
Dec 10, 2001
OXOID PYLORI TEST KIT, MODEL DR0130M
Microbiology
122d
Cleared
Apr 24, 2001
MOXIFLOXACIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
Microbiology
60d
Cleared
Apr 24, 2001
LINEZOLID ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
Microbiology
60d
Cleared
May 22, 2000
GATIFLOXACIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
Microbiology
61d
Cleared
May 15, 2000
QUINUPRISTIN/DALFOPRISTIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
Microbiology
54d
Cleared
Feb 28, 2000
DRYSPOT E.COLI 0157 KIT
Microbiology
143d
Cleared
Apr 02, 1999
TROVAFLOXACIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
Microbiology
105d
Cleared
Mar 09, 1999
GENTAMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
Microbiology
71d