MEE-1000A NEUROMASTER

MEE-1000A NEUROMASTER is an FDA 510(k)-cleared medical device (K051178) manufactured by Nihon Kohden America, 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 16, 2005. Regulation: 8.