Siemens Medical Systems USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Siemens Medical Systems USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cios Spin, Cios Alpha
2
Total
2
Cleared
0
Denied
Siemens Medical Systems USA, Inc. has 2 FDA 510(k) cleared medical devices. Based in Malvern, US.
Last cleared in 2021. Active since 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Siemens Medical Systems USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Siemens Healthcare GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Siemens Medical Systems USA, Inc.
2 devices