VAXIOM FAMILY OF RF LESION PROBES & ELEC

VAXIOM FAMILY OF RF LESION PROBES & ELEC is an FDA 510(k)-cleared medical device (K802243) manufactured by Progress Mankind Technology. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 11, 1980. Regulation: 8.