CLARISSA INFANT NCPAP CANNULA

CLARISSA INFANT NCPAP CANNULA is an FDA 510(k)-cleared medical device (K032922) manufactured by Airways Ltd., 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 September 21, 2004. Regulation: 8.