Hudson RCI Triflo II Incentive Deep Breathing Exerciser

Hudson RCI Triflo II Incentive Deep Breathing Exerciser is an FDA 510(k)-cleared medical device (K220565) manufactured by Medline Industries, 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 24, 2022. Regulation: 8.