NEURO-PULSER 2 TRANSCUTAN. ELEC. NERVE

NEURO-PULSER 2 TRANSCUTAN. ELEC. NERVE is an FDA 510(k)-cleared medical device (K831850) manufactured by Th Charters, 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 July 18, 1983. Regulation: 8.