ACTION STORM RANGER II, ACTION STORM POWER 9000

ACTION STORM RANGER II, ACTION STORM POWER 9000 is an FDA 510(k)-cleared medical device (K982064) manufactured by Invacare Corp.. 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 October 4, 1998. Regulation: 8.