DEVILBISS MODEL 8500D

DEVILBISS MODEL 8500D is an FDA 510(k)-cleared medical device (K874041) manufactured by The Devilbiss Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 22, 1987. Regulation: 8.