OXYGEN GENERATOR LIQUEFIER - (OGL)

OXYGEN GENERATOR LIQUEFIER - (OGL) is an FDA 510(k)-cleared medical device (K131990) manufactured by Essex Cryogenics of Missouri, 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 20, 2014. Regulation: 8.