FOGARTY ARTERIAL EMBOLECTOMY II CATHETER

FOGARTY ARTERIAL EMBOLECTOMY II CATHETER is an FDA 510(k)-cleared medical device (K901625) manufactured by Baxter Healthcare 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 July 5, 1990. Regulation: 8.