NORTEC ROBERTAZZI NASOPHARYNGEAL AIRWAY

NORTEC ROBERTAZZI NASOPHARYNGEAL AIRWAY is an FDA 510(k)-cleared medical device (K911784) manufactured by North American Sterilization & Packaging Co.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 22, 1991. Regulation: 8.