CORDIPAK CARDIAC CATHETERIZATION PACK

CORDIPAK CARDIAC CATHETERIZATION PACK is an FDA 510(k)-cleared medical device (K863337) manufactured by Angi-Pak 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 September 28, 1986. Regulation: 8.