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
1741124380
Device Listing 1741124380
Listing Summary
#
Listing key
1741124380
Premarket submission
K142629
Device
EG-530CT, EG-530D, EC-530DL, and ES-530WE Endoscopes
Applicant
Fujifilm Medical System U.S.A., Inc.
Product code
FDS
Decision date
2015-05-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
10914
3001722928
3001722928
FUJIFILM CORPORATION
1
N
2026-01-01
798 MIYANODAI KAISEI-MACHI ASHIGARAKAMI-GUN Kanagawa JP 258-8538
122261
3008178481
3010516924
FUJIFILM Techno Products Co., LTD. Mito Site
1
N
2020-04-25
4112 Tono Hitachiomiya City Ibaraki JP 319-2224