Rulo Radiofrequency Lesion Probe

Rulo Radiofrequency Lesion Probe is an FDA 510(k)-cleared medical device (K190256) manufactured by Epimed International, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 7, 2019. Regulation: 8.