AMPLAID MARK 4 AND MARK 5

AMPLAID MARK 4 AND MARK 5 is an FDA 510(k)-cleared medical device (K781667) manufactured by Amplaid USA, 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 November 2, 1978. Regulation: 8.