Medical Device Manufacturer · US , Washington , DC

Leibinger GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1994

Total

Cleared

Denied

Leibinger GmbH has 3 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 3 cleared submissions from 1994 to 1997.

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

FDA 510(k) Regulatory Record - Leibinger GmbH

3 devices

1-3 of 3