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
1653469149
Device Listing 1653469149
Listing Summary
#
Listing key
1653469149
Premarket submission
K984634
Device
3D-ANGIO
Applicant
Siemens Medical Corp.
Product code
JAK
Decision date
1999-03-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
8876
3004977335
3004977335
Robert Phillips
1
N
2026-01-01
40 Liberty Boulevard MALVERN PA US 19355