DEVILBISS MODEL 5500

DEVILBISS MODEL 5500 is an FDA 510(k)-cleared medical device (K946095) 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 August 23, 1995. Regulation: 8.