Medical Device Manufacturer · US , Telford , PA

Drager Medical AG & Co. Kgaa - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2005

Total

Cleared

Denied

Drager Medical AG & Co. Kgaa has 3 FDA 510(k) cleared medical devices. Based in Telford, US.

Historical record: 3 cleared submissions from 2005 to 2010. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Drager Medical AG & Co. Kgaa Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Drager Medical AG & Co. Kgaa

3 devices

1-3 of 3