CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA.

CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA. is an FDA 510(k)-cleared medical device (K863469) manufactured by Cordis Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 19, 1987. Regulation: 8.