ARTERIAL EMBOLECTOMY CATHETER (MODIFIED)

ARTERIAL EMBOLECTOMY CATHETER (MODIFIED) is an FDA 510(k)-cleared medical device (K790838) manufactured by Shiley, 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 June 10, 1979. Regulation: 8.