DEVILBISS MODEL 7351 SERIES

DEVILBISS MODEL 7351 SERIES is an FDA 510(k)-cleared medical device (K894424) 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 September 17, 1989. Regulation: 8.