VERIMED MYOEXORCISER VERISTIM

VERIMED MYOEXORCISER VERISTIM is an FDA 510(k)-cleared medical device (K893220) manufactured by Verimed Holdings, 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 March 6, 1990. Regulation: 8.