GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP

GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP is an FDA 510(k)-cleared medical device (K761169) manufactured by Pilling Co.. 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 8, 1976. Regulation: 8.