DeVilbiss Intellipap2/DeVilbiss BLUE

DeVilbiss Intellipap2/DeVilbiss BLUE is an FDA 510(k)-cleared medical device (K143677) manufactured by Devilbiss Healthcare, LLC. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 17, 2015. Regulation: 8.