SILICONE RUBBER-BI NASOPHARYNGEAL AIR

SILICONE RUBBER-BI NASOPHARYNGEAL AIR is an FDA 510(k)-cleared medical device (K792018) manufactured by Vesta, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 12, 1979. Regulation: 8.