Medical Device Manufacturer · US , Washington , DC

Seidel Medizin GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987

Total

Cleared

Denied

Seidel Medizin GmbH has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 1987 to 1996. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Seidel Medizin GmbH Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Seidel Medizin GmbH

2 devices

1-2 of 2