
Neuromusclar Electrical Stimulation Systems, Ltd.
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HANDMASTER is an FDA 510(k)-cleared medical device (K010837) manufactured by Neuromusclar Electrical Stimulation Systems, 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 June 14, 2001. Regulation: 8.