WHISPER SWIVEL II EXHALATION PORT

WHISPER SWIVEL II EXHALATION PORT is an FDA 510(k)-cleared medical device (K962203) manufactured by Respironics, 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 December 4, 1996. Regulation: 8.