VORTEX VALVED HOLDING CHAMBER

VORTEX VALVED HOLDING CHAMBER is an FDA 510(k)-cleared medical device (K020944) manufactured by Pari Innovative Manufacturers, 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 May 8, 2002. Regulation: 8.