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
1231231891
Device Listing 1231231891
Listing Summary
#
Listing key
1231231891
Premarket submission
K231941
Device
ARIETTA x10
Applicant
FUJIFILM Healthcare Americas Corporation
Product code
IYN
Decision date
2023-11-20
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
294287
3019784575
3019784575
FUJIFILM Corporation Medical Systems Research & Development Center Kokubunji
1
N
2026-01-01
3-1-1 HIGASHIKOIGAKUBO KOKUBUNJI-SHI T?ky? JP 185-0014
330648
3032109225
3032109225
FUJIFILM Healthcare Manufacturing Corporation Kashiwa Office
1
N
2026-01-01
2-1, Shintoyofuta Kashiwa-shi Chiba JP 277-0804