RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR

RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR is an FDA 510(k)-cleared medical device (K853083) manufactured by Home Medical Supply, 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 September 2, 1985. Regulation: 8.