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
2008593003
Device Listing 2008593003
Listing Summary
#
Listing key
2008593003
Premarket submission
K955012
Device
MIZUHO RADIOLUCENT HEAD FRAME
Applicant
Mizuho America, Inc.
Product code
HBL
Decision date
1996-09-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
46849
9680242
3009504761
MIZUHO Corporation Gosen Factory
1
N
2027-01-01
3631-14 Akomi Gosen Niigata JP 959-1821
202420
3011547624
3011547624
MIZUHO CORPORATION
1
N
2027-01-01
3-30-13 HONGO BUNKYO-KU Tokyo JP 1130033