UNI-GRAFT K DV VASCULAR GRAFT

UNI-GRAFT K DV VASCULAR GRAFT is an FDA 510(k)-cleared medical device (K991813) manufactured by Atrium Medical Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 31, 1999. Regulation: 8.