Siemens Medical Soultions USA, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
syngo.via MI Workflows VB40A, Scenium Ref K191309
Regimes: 510(k) Registry: 510(k)syngo.CT Cardiac Planning Ref K200515
Regimes: 510(k) Registry: 510(k)Chondral Quant Ref K231351
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Siemens Medical Soultions USA, Inc. have in the registry?
The registry currently lists 3 devices for Siemens Medical Soultions USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Siemens Medical Soultions USA, Inc.'s devices?
Among its 3 most recently registered devices, Siemens Medical Soultions USA, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Siemens Medical Soultions USA, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Siemens Medical Soultions USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Siemens Medical Soultions USA, Inc. in the registry?
The most recently registered devices listed for Siemens Medical Soultions USA, Inc. include syngo.via MI Workflows VB40A, Scenium, syngo.CT Cardiac Planning and Chondral Quant.