Medical Device Manufacturer · FR , Chassieu

Renishaw Mayfield Sarl - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2014

Total

Cleared

Denied

Renishaw Mayfield Sarl has 3 FDA 510(k) cleared medical devices. Based in Chassieu, FR.

Historical record: 3 cleared submissions from 2014 to 2018. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Renishaw Mayfield Sarl Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Renishaw Mayfield Sarl

3 devices

1-3 of 3