VISUAL PATTERN REVERSAL GEN. & PHOTIC S.

VISUAL PATTERN REVERSAL GEN. & PHOTIC S. is an FDA 510(k)-cleared medical device (K810481) 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 March 10, 1981. Regulation: 8.