MISTY OX LAMINAR DIFFUSER HUMIDIFIER

MISTY OX LAMINAR DIFFUSER HUMIDIFIER is an FDA 510(k)-cleared medical device (K923754) manufactured by Medical Molding Corp. of America. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 6, 1992. Regulation: 8.