Medical Device Manufacturer · FI , Helsinki

Elekta Neuromag OY - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2004

Total

Cleared

Denied

Elekta Neuromag OY has 4 FDA 510(k) cleared medical devices. Based in Helsinki, FI.

Historical record: 4 cleared submissions from 2004 to 2010. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Elekta Neuromag OY Filter by specialty or product code using the sidebar.

Elekta Neuromag OY is one of 32 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Elekta Neuromag OY

4 devices

1-4 of 4