Oxoid U.S.A., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oxoid U.S.A., Inc. - FDA 510(k) Cleared Devices
93
Total
93
Cleared
0
Denied
Oxoid U.S.A., Inc. has 93 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 93 cleared submissions from 1980 to 1989.
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 U.S.A., Inc.
93 devices
Cleared
Jun 09, 1989
LISTERIA SELECTIVE ENRICHMENT MEDIUM
Microbiology
81d
Cleared
Feb 03, 1989
ESCHERICHIA COLI 0157 LATEX AGGLUTINATION TEST KIT
Microbiology
133d
Cleared
Oct 25, 1988
LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)
Microbiology
19d
Cleared
Nov 06, 1987
STAPHYLASE TEST
Microbiology
17d
Cleared
Aug 10, 1987
SORBITOL MACCONKEY AGAR NO. 3 CM 813
Microbiology
12d
Cleared
Jun 15, 1987
MCBRIDE MEDIUM CM 819
Microbiology
12d
Cleared
Jun 10, 1987
RABBIT PLASMA FIBRINOGEN SUPPLEMENT SR 122
Microbiology
93d
Cleared
Nov 05, 1986
OXOID SIGNAL BLOOD CULTURE SYSTEM
Microbiology
92d
Cleared
Nov 04, 1986
DIAGNOSTIC REAGENT SET-RPLA
Microbiology
308d
Cleared
Nov 04, 1986
DIAGNOSTIC REAGENT VET-RPLA
Microbiology
308d
Cleared
Nov 04, 1986
DIAGNOSTIC REAGENT PET-RPLA
Microbiology
308d
Cleared
Nov 04, 1986
DIAGNOSTIC REAGENT TST-RPLA
Microbiology
308d
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