VENOUS RETURN CANNULA W/CUFF 91039

VENOUS RETURN CANNULA W/CUFF 91039 is an FDA 510(k)-cleared medical device (K854487) manufactured by Dlp, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 9, 1986. Regulation: 8.