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
1339176275
Device Listing 1339176275
Listing Summary
#
Listing key
1339176275
Premarket submission
K810931
Device
SS AGAR (MODIFIED)
Applicant
Oxoid U.S.A., Inc.
Product code
JSI
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