CHALLENGE 3000 NEUROLOGICAL BOOSTER

CHALLENGE 3000 NEUROLOGICAL BOOSTER is an FDA 510(k)-cleared medical device (K903148) manufactured by Maximum Performance Technologies, Mpts, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 9, 1991. Regulation: 8.