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
1523847501
Device Listing 1523847501
Listing Summary
#
Listing key
1523847501
Premarket submission
K980695
Device
FUJI I
Applicant
GC America, Inc.
Product code
EMA
Decision date
1998-04-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
198413
3012421607
3012421607
MAINLINE MEDICAL DENTAL SUPPLY
1
N
2026-01-01
100-102 Rossdean Dr North York Ontario CA M9L 2S1