VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B

VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B is an FDA 510(k)-cleared medical device (K900115) manufactured by Ventlab Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 21, 1990. Regulation: 8.