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
1862384421
Device Listing 1862384421
Listing Summary
#
Listing key
1862384421
Premarket submission
K160369
Device
GuideWire
Applicant
Fiagon GmbH
Product code
PGW
Decision date
2016-03-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
171354
3010313588
3010313588
Fiagon GMBH
1
N
2026-01-01
Neuendorfstr. 23b Hennigsdorf Brandenburg DE 16761