VORTRAN GO2VENT

VORTRAN GO2VENT is an FDA 510(k)-cleared medical device (K162968) manufactured by Vortran Medical Technology 1, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 9, 2017. Regulation: 8.