NEURO N 50 LESION GENERATOR

NEURO N 50 LESION GENERATOR is an FDA 510(k)-cleared medical device (K896450) manufactured by Leibinger & Fischer , Ltd.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 18, 1991. Regulation: 8.