BELMONT MODEL PBP INTRA-AORTIC BALLOON PUMP

BELMONT MODEL PBP INTRA-AORTIC BALLOON PUMP is an FDA 510(k)-cleared medical device (K915580) manufactured by Belmont Instrument 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 October 29, 1992. Regulation: 8.