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Oxoid U.S.A., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
93
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMJune 9, 1989
K884026ESCHERICHIA COLI 0157 LATEX AGGLUTINATION TEST KITFebruary 3, 1989
K884208LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)October 25, 1988
K874303STAPHYLASE TESTNovember 6, 1987
K872956SORBITOL MACCONKEY AGAR NO. 3 CM 813August 10, 1987
K872135MCBRIDE MEDIUM CM 819June 15, 1987
K870945RABBIT PLASMA FIBRINOGEN SUPPLEMENT SR 122June 10, 1987
K862946OXOID SIGNAL BLOOD CULTURE SYSTEMNovember 5, 1986
K855235DIAGNOSTIC REAGENT PET-RPLANovember 4, 1986
K855234DIAGNOSTIC REAGENT VET-RPLANovember 4, 1986
K855233DIAGNOSTIC REAGENT SET-RPLANovember 4, 1986
K855236DIAGNOSTIC REAGENT TST-RPLANovember 4, 1986
K854929OXOID STREPTOCOCAL GROUPING KITMarch 11, 1986
K860153OXOID ANTIMICROBIAL SUSCEPTIBILITY DISCSMarch 4, 1986
K850832CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQMarch 29, 1985
K850658CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEMarch 20, 1985
K844887IDENTIFICATION STICKS OXIDASEFebruary 25, 1985
K841659DRIGALSKI LITMUS LACTOSE AGARJune 7, 1984
K841662MAXIMUM RECOVERY DILUENTJune 7, 1984
K841660SELENITE CYSTINE BROTH BASEMay 14, 1984