Siemens AG Healthcare is one of 472 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Siemens AG Healthcare - FDA 510(k) Cleared Devices
Recent clearances: SYNGO.PLAZA VB10A
1
Total
1
Cleared
0
Denied
Siemens AG Healthcare has 1 FDA 510(k) cleared medical devices. Based in Erlangen, DE.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Siemens AG Healthcare Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Siemens AG Healthcare
1 devices