INTRA-AORTIC BALLOON PUMP MODEL KAAT

INTRA-AORTIC BALLOON PUMP MODEL KAAT is an FDA 510(k)-cleared medical device (K875036) 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 May 17, 1988. Regulation: 8.