DEVILBISS MODEL PV02 SERIES

DEVILBISS MODEL PV02 SERIES is an FDA 510(k)-cleared medical device (K896457) 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 January 31, 1990. Regulation: 8.