CARDIMA VUEPORT CORONARY SINUS BALLOON OCCLUSION GUIDING CATHETER

CARDIMA VUEPORT CORONARY SINUS BALLOON OCCLUSION GUIDING CATHETER is an FDA 510(k)-cleared medical device (K973298) manufactured by Cardima, 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 25, 1998. Regulation: 8.