VYGON DOUBLE LUMEN ENDOTRACHEAL TUBE

VYGON DOUBLE LUMEN ENDOTRACHEAL TUBE is an FDA 510(k)-cleared medical device (K960795) manufactured by Vygon Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 21, 1996. Regulation: 8.