CHASE CORONARY OSTIAL PERFUSION CANNULA

CHASE CORONARY OSTIAL PERFUSION CANNULA is an FDA 510(k)-cleared medical device (K971041) manufactured by Chase 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 May 12, 1997. Regulation: 8.