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
1919233517
Device Listing 1919233517
Listing Summary
#
Listing key
1919233517
Premarket submission
K261713
Device
Synapse PACS (7.6.0)
Applicant
FUJIFILM Healthcare Americas Corporation
Product code
QIH
Decision date
2026-06-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
97105
3004972322
3004972322
FUJIFILM Healthcare Americas Corporation
1
Y
2026-01-01
79 TW Alexander Drive, Building 4501 Durham NC US 27709