FT2000 SEQUENCER FOR MUSCLE STIMULATOR

FT2000 SEQUENCER FOR MUSCLE STIMULATOR is an FDA 510(k)-cleared medical device (K050595) manufactured by Midwest Development. 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 22, 2005. Regulation: 8.