Siemens Medical Solutions USA, Inc. Ultrasound Gro
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
Acuson S1000 / S2000 / S3000 Ref K132804
Regimes: 510(k) Registry: 510(k)Acuson SC2000 Diagnostic Ultrasound System Ref K132654
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Siemens Medical Solutions USA, Inc. Ultrasound Gro have in the registry?
The registry currently lists 3 devices for Siemens Medical Solutions USA, Inc. Ultrasound Gro. Devices recorded under merged duplicate company entries are counted once.
Which registries list Siemens Medical Solutions USA, Inc. Ultrasound Gro's devices?
Among its 3 most recently registered devices, Siemens Medical Solutions USA, Inc. Ultrasound Gro has devices listed in FDA 510(k) (3 devices).
What risk classes do Siemens Medical Solutions USA, Inc. Ultrasound Gro's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Siemens Medical Solutions USA, Inc. Ultrasound Gro's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Siemens Medical Solutions USA, Inc. Ultrasound Gro in the registry?
The most recently registered devices listed for Siemens Medical Solutions USA, Inc. Ultrasound Gro include ACUSON S1000 / S2000 / S3000, ACUSON SC2000 DIAGNOSTIC ULTRASOUND SYSTEM and ACUSON X150 DIAGNOSTIC ULTRASOUND SYSTEM SONOVISTA X150 DIAGNOSTIC ULTRASOUND SYSTEM.