MIRAGE FULL FACE MASK SERIES 2

MIRAGE FULL FACE MASK SERIES 2 is an FDA 510(k)-cleared medical device (K023284) manufactured by Resmed, Ltd.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 26, 2002. Regulation: 8.