ESCOTEK EST 220 INTERFERENCE THERAPY UNIT

ESCOTEK EST 220 INTERFERENCE THERAPY UNIT is an FDA 510(k)-cleared medical device (K844388) manufactured by Nor-Am Patient Care Products, 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 6, 1985. Regulation: 8.