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.

Ndd Medizitechnik AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ndd Medizitechnik AG

3 devices

1-3 of 3