SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH

SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH is an FDA 510(k)-cleared medical device (K891458) manufactured by Back IN Action, 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 October 19, 1989. Regulation: 8.