Medical Device Manufacturer · US , Mchenry , IL

Dragerwerk AG - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1980

Total

Cleared

Denied

Dragerwerk AG has 3 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 3 cleared submissions from 1980 to 1991. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Dragerwerk AG

3 devices

1-3 of 3