Siemens Healthcare is one of 16378 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Siemens Healthcare - FDA 510(k) Cleared Devices
Recent clearances: ACUSON S3000 S2000 S1000 Diagnostic Ultrasound Systems
1
Total
1
Cleared
0
Denied
Siemens Healthcare has 1 FDA 510(k) cleared medical devices. Based in Issaquah, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Siemens Healthcare 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 Healthcare
1 devices