Siemens Medical Systems USA, Inc. - FDA 510(k) Cleared Devices
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