10.5 FRENCH PERCUTANEOUS DOUBLE LUMEN INTRA-AORTIC

10.5 FRENCH PERCUTANEOUS DOUBLE LUMEN INTRA-AORTIC is an FDA 510(k)-cleared medical device (K882274) 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 March 19, 1989. Regulation: 8.