KENDALL CURITY ENDOTRACHEAL TUBES

KENDALL CURITY ENDOTRACHEAL TUBES is an FDA 510(k)-cleared medical device (K892432) manufactured by The Kendal Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 11, 1989. Regulation: 8.