COMPRESSED AIR & OXYGEN GEN./DELIVERY SY

COMPRESSED AIR & OXYGEN GEN./DELIVERY SY is an FDA 510(k)-cleared medical device (K803232) manufactured by Dri-Aire, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 1, 1981. Regulation: 8.