AEROCHAMBER W/MASK, MODIFIED

AEROCHAMBER W/MASK, MODIFIED is an FDA 510(k)-cleared medical device (K930574) manufactured by Monaghan Medical 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 January 23, 1994. Regulation: 8.