Medical Device Manufacturer · DE , Freiburg

Stockert GmbH - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2001

Total

Cleared

Denied

Stockert GmbH has 5 FDA 510(k) cleared medical devices. Based in Freiburg, DE.

Historical record: 5 cleared submissions from 2001 to 2007. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Stockert GmbH

5 devices

1-5 of 5