INFANT NASAL CANNULAE ASSEMBLY

INFANT NASAL CANNULAE ASSEMBLY is an FDA 510(k)-cleared medical device (K841773) manufactured by Ackrad Laboratories. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 25, 1984. Regulation: 8.