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
1159345750
Device Listing 1159345750
Listing Summary
#
Listing key
1159345750
Premarket submission
K902734
Device
PR CANNULAS
Applicant
Olympus Corp.
Product code
FGE
Decision date
1990-08-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
37024
2951238
1000635022
Olympus Corporation of the Americas
1
N
2020-04-25
2400 RINGWOOD AVE. SAN JOSE CA US 95131