CURITY FIBEROPTIC INTUBATING AIRWAY

CURITY FIBEROPTIC INTUBATING AIRWAY is an FDA 510(k)-cleared medical device (K855137) manufactured by The Kendal Co.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 10, 1986. Regulation: 8.