PLEUR-EVAC PLUS CONTIN. REINFUS. & AUTOINFUS. SYST

PLEUR-EVAC PLUS CONTIN. REINFUS. & AUTOINFUS. SYST is an FDA 510(k)-cleared medical device (K911656) manufactured by Pfizer Hospital Products Group, 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 August 12, 1991. Regulation: 8.