VERIMED MYOEXORCISER III (MYO III)

VERIMED MYOEXORCISER III (MYO III) is an FDA 510(k)-cleared medical device (K892649) manufactured by Verimed Holdings, 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 December 12, 1989. Regulation: 8.