SENSORY NEEDLE ELECTRODE DNE 111-115,116-117,118

SENSORY NEEDLE ELECTRODE DNE 111-115,116-117,118 is an FDA 510(k)-cleared medical device (K894911) manufactured by Dantec Electronics, 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 13, 1990. Regulation: 8.