40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER

40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER is an FDA 510(k)-cleared medical device (K864567) manufactured by Aries Medical, 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 May 11, 1987. Regulation: 8.