Renishaw Mayfield Sarl is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Renishaw Mayfield Sarl - FDA 510(k) Cleared Devices
Recent clearances: neuromate Gen III, neuromate Gen III
3
Total
3
Cleared
0
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