VENTURE HOME FILL II, MODEL IOH 200

VENTURE HOME FILL II, MODEL IOH 200 is an FDA 510(k)-cleared medical device (K003939) manufactured by Invacare Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 20, 2001. Regulation: 8.