Medical Device Manufacturer · DE , L?beck

Dragerwerk AG & CO Kgaa - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2019

Total

Cleared

Denied

Dragerwerk AG & CO Kgaa has 2 FDA 510(k) cleared medical devices. Based in L?beck, DE.

Historical record: 2 cleared submissions from 2019 to 2019. Primary specialty: Anesthesiology.

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

FDA 510(k) cleared devices by Dragerwerk AG & CO Kgaa

2 devices

1-2 of 2