SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M

SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M is an FDA 510(k)-cleared medical device (K960754) manufactured by Mecta Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 17, 1996. Regulation: 8.