DEVILBISS NEBULIZER MODEL 800

DEVILBISS NEBULIZER MODEL 800 is an FDA 510(k)-cleared medical device (K993492) manufactured by Sunrise Medical Hhg, 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 April 20, 2000. Regulation: 8.