VERSA-STIM ELECTRODE LINE MODIFIED

VERSA-STIM ELECTRODE LINE MODIFIED is an FDA 510(k)-cleared medical device (K911069) manufactured by Conmedcorp. 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 15, 1991. Regulation: 8.