Medical Device Manufacturer · US , Telford , PA

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

2 submissions · 2 cleared · Since 2004

Total

Cleared

Denied

Draeget Medical AG & Co. Kgaa has 2 FDA 510(k) cleared medical devices. Based in Telford, US.

Historical record: 2 cleared submissions from 2004 to 2004. Primary specialty: Anesthesiology.

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

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

2 devices

1-2 of 2