HANDMASTER NMS1

HANDMASTER NMS1 is an FDA 510(k)-cleared medical device (K982482) manufactured by N.E.S.S. Nuromuscular Electrical Stimulation Syst. 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 September 29, 1998. Regulation: 8.