MODEL RFG-3C RADIOFREQUENCY LESION GENERATOR

MODEL RFG-3C RADIOFREQUENCY LESION GENERATOR is an FDA 510(k)-cleared medical device (K901540) manufactured by Radionics, 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 April 7, 1991. Regulation: 8.