BONHAWA Respiratory Humidifier

BONHAWA Respiratory Humidifier is an FDA 510(k)-cleared medical device (K223863) manufactured by Telesair, 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 October 12, 2023. Regulation: 8.