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.

Siemens Burdick, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Siemens Burdick, Inc.

7 devices

1-7 of 7