PURITAN BENNETT 980 SERIES VENTILATOR SYSTEM

PURITAN BENNETT 980 SERIES VENTILATOR SYSTEM is an FDA 510(k)-cleared medical device (K131252) manufactured by Covidien. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 23, 2014. Regulation: 8.