PMH 5000 HEATED HUMIDIFIER FOR RESPIRATORY THERAPY

PMH 5000 HEATED HUMIDIFIER FOR RESPIRATORY THERAPY is an FDA 510(k)-cleared medical device (K020700) manufactured by Pegasus Research 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 April 25, 2004. Regulation: 8.