MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER

MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER is an FDA 510(k)-cleared medical device (K050371) manufactured by Medrad, 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 June 6, 2005. Regulation: 8.