DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12

DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12 is an FDA 510(k)-cleared medical device (K896874) manufactured by Dantec Medical, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 17, 1990. Regulation: 8.