Medical Device Manufacturer · US , Andover , MA

Ndd Medizitechnik AG - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2009

Total

Cleared

Denied

Ndd Medizitechnik AG has 3 FDA 510(k) cleared medical devices. Based in Andover, US.

Historical record: 3 cleared submissions from 2009 to 2012. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Ndd Medizitechnik AG

3 devices

1-3 of 3