CATHETER, ARTERIAL EMBOLECTOMY

CATHETER, ARTERIAL EMBOLECTOMY is an FDA 510(k)-cleared medical device (K770714) manufactured by Mallinckrodt Critical Care. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 26, 1977. Regulation: 8.