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
1731724715
Device Listing 1731724715
Listing Summary
#
Listing key
1731724715
Premarket submission
K910757
Device
THE BULLION
Applicant
Octostop, Inc.
Product code
KPR
Decision date
1991-09-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
40741
8022065
3003434037
OCTOSTOP, INC.
1
N
2026-01-01
1675 BOUL ST-ELZEAR OUEST LAVAL Quebec CA H7L 3N6