DEVILBISS MODEL 5000

DEVILBISS MODEL 5000 is an FDA 510(k)-cleared medical device (K911896) manufactured by Devilbiss Health Care, 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 July 30, 1991. Regulation: 8.