MEDTRON TYPE P-300 ULTRASONIC THERAPY UNIT

MEDTRON TYPE P-300 ULTRASONIC THERAPY UNIT is an FDA 510(k)-cleared medical device (K861864) manufactured by I-Rep, 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 July 13, 1986. Regulation: 8.