Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1195211690
Device Listing 1195211690
Listing Summary
#
Listing key
1195211690
Premarket submission
K810932
Device
VITOX
Applicant
Oxoid U.S.A., Inc.
Product code
JSK
Decision date
1981-04-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
185464
8010096
3006224287
OXOID, LTD.
1
N
2026-01-01
WADE RD. BASINGSTOKE, HAMPSHIRE GB RG24 8PW