DANTEC MAGNETIC STIMULATOR MAGPRO

DANTEC MAGNETIC STIMULATOR MAGPRO is an FDA 510(k)-cleared medical device (K926516) manufactured by Dantec 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 30, 1993. Regulation: 8.