VORTRAN GO2VENT with PEEP Valve

VORTRAN GO2VENT with PEEP Valve is an FDA 510(k)-cleared medical device (K202219) 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 February 10, 2021. Regulation: 8.