Siemens Medical Solutions USA, Inc. Ultrasound Gro is one of 13678 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Siemens Medical Solutions USA, Inc. Ultrasound Gro - FDA 510(k) Clear...
Recent clearances: ACUSON S1000 / S2000 / S3000, ACUSON SC2000 DIAGNOSTIC ULTRASOUND SYSTEM, ACUSON X150 DIAGNOSTIC ULTRASOUND SYSTEM SONOVISTA X150 DIAGNOSTIC ULTRASOUND SYSTEM
3
Total
3
Cleared
0
Denied
Siemens Medical Solutions USA, Inc. Ultrasound Gro has 3 FDA 510(k) cleared medical devices. Based in Moutain View, US.
Historical record: 3 cleared submissions from 2012 to 2013. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Siemens Medical Solutions USA, Inc. Ultrasound Gro Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Siemens Medical Solutions USA, Inc. Ultrasound Gro
3 devices