OMNISTIM II COMBIN. THERAPY SYS

OMNISTIM II COMBIN. THERAPY SYS is an FDA 510(k)-cleared medical device (K843351) manufactured by Physio Technology, 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 September 17, 1984. Regulation: 8.