MEDIUM FREQU. ELEC. MUSCLE STIMULATOR

MEDIUM FREQU. ELEC. MUSCLE STIMULATOR is an FDA 510(k)-cleared medical device (K850698) manufactured by Chattanooga Group, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 16, 1985. Regulation: 8.