NEURAL MAGNETIC STIMULATOR, THE D190

NEURAL MAGNETIC STIMULATOR, THE D190 is an FDA 510(k)-cleared medical device (K883340) manufactured by Tracor Northern, 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 December 28, 1988. Regulation: 8.