CANNULAS, DYNACOR'S NASAL OXYGEN

CANNULAS, DYNACOR'S NASAL OXYGEN is an FDA 510(k)-cleared medical device (K790056) manufactured by Medline Industries, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 4, 1979. Regulation: 8.