ARIES 40CC PERCU. (D/L) INTRA-AORTIC BALLOON CATH.

ARIES 40CC PERCU. (D/L) INTRA-AORTIC BALLOON CATH. is an FDA 510(k)-cleared medical device (K882289) 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 December 11, 1988. Regulation: 8.