CATHETERS, ARTERIAL EMBOLECTOMY

CATHETERS, ARTERIAL EMBOLECTOMY is an FDA 510(k)-cleared medical device (K780244) manufactured by Extracorporeal Medical Specialities, 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 April 12, 1978. Regulation: 8.