KIMSTIM AURICULAR ELECTRODE

KIMSTIM AURICULAR ELECTRODE is an FDA 510(k)-cleared medical device (K011691) manufactured by Kim Institute For Rehabilitation Medicine, P.C.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 26, 2001. Regulation: 8.