PERCOR INTRA-AORTIC BALLOON INSERTION

PERCOR INTRA-AORTIC BALLOON INSERTION is an FDA 510(k)-cleared medical device (K823342) manufactured by Datascope Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 23, 1983. Regulation: 8.