DUAL SERVO HEATED RESPIRATORY HUMIDIFIER

DUAL SERVO HEATED RESPIRATORY HUMIDIFIER is an FDA 510(k)-cleared medical device (K822816) manufactured by Fisher & Paykel Allied Products , Ltd.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 21, 1982. Regulation: 8.