DEVILBISS PD1000

DEVILBISS PD1000 is an FDA 510(k)-cleared medical device (K020329) manufactured by Sunrise Medical Hhg, 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 June 18, 2002. Regulation: 8.