GAS-VAK(R), MODEL 300

GAS-VAK(R), MODEL 300 is an FDA 510(k)-cleared medical device (K890438) manufactured by Gas-Vak. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 6, 1989. Regulation: 8.