AVE 4F SITESEER CARDIOVASCULAR ANGIOGRAPHIC CATHETER

AVE 4F SITESEER CARDIOVASCULAR ANGIOGRAPHIC CATHETER is an FDA 510(k)-cleared medical device (K984627) manufactured by Arterial Vascular Engineering, 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 July 26, 1999. Regulation: 8.