DEVILBISS MODEL 7352 SERIES

DEVILBISS MODEL 7352 SERIES is an FDA 510(k)-cleared medical device (K904766) 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 March 25, 1991. Regulation: 8.