RHYTHM TOUCH Q 2-WAY

RHYTHM TOUCH Q 2-WAY is an FDA 510(k)-cleared medical device (K063743) manufactured by Shockim Enterprises, Ltd.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 23, 2007. Regulation: 8.