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
2039778139
Device Listing 2039778139
Listing Summary
#
Listing key
2039778139
Premarket submission
K220432
Device
ARTIS icono (VE21) System
Applicant
Siemens Medical Solutions USA, Inc.
Product code
OWB
Decision date
2022-06-29
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