DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE

DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE is an FDA 510(k)-cleared medical device (K823002) manufactured by Tri W-G, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 16, 1982. Regulation: 8.