9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOON

9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOON is an FDA 510(k)-cleared medical device (K892222) manufactured by Kontron Instruments, 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 September 13, 1990. Regulation: 8.