MODIFICATION PURITAN BENETT COMPANION 2801 VOL VEN

MODIFICATION PURITAN BENETT COMPANION 2801 VOL VEN is an FDA 510(k)-cleared medical device (K915312) manufactured by Puritan Bennett Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 7, 1992. Regulation: 8.