NORTECH MODEL 87202204 ELECTRODE

NORTECH MODEL 87202204 ELECTRODE is an FDA 510(k)-cleared medical device (K903554) manufactured by Medtronic Andover Medical, 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 August 29, 1990. Regulation: 8.