MEDISONIC HUMDIFIER/INHALER

MEDISONIC HUMDIFIER/INHALER is an FDA 510(k)-cleared medical device (K901114) manufactured by Medisonic U.S.A., 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 May 21, 1990. Regulation: 8.