PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE

PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE is an FDA 510(k)-cleared medical device (K851024) manufactured by Pfizer, 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 May 22, 1985. Regulation: 8.