INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2

INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2 is an FDA 510(k)-cleared medical device (K921612) manufactured by Medstar, 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 17, 1992. Regulation: 8.