Medical Device Manufacturer · US , Miltoon , WI

Siemens Burdick, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1991

Total

Cleared

Denied

Siemens Burdick, Inc. has 7 FDA 510(k) cleared medical devices. Based in Miltoon, US.

Historical record: 7 cleared submissions from 1991 to 1992. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Siemens Burdick, Inc. Filter by specialty or product code using the sidebar.

7 devices

1–7 of 7

Data Source

FDA 510(k) public files . 174,402 total devices indexed.