DITER ULTRASONIC S 3000

DITER ULTRASONIC S 3000 is an FDA 510(k)-cleared medical device (K901950) manufactured by Diter Elektroniikka OY. 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 26, 1990. Regulation: 8.