CUTANEOUS ELECTROTHERAPY AND RECORDING ELECTRODES; TENS ELECTRODES

CUTANEOUS ELECTROTHERAPY AND RECORDING ELECTRODES; TENS ELECTRODES is an FDA 510(k)-cleared medical device (K070807) manufactured by Pepin Mfg., 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 May 22, 2007. Regulation: 8.