ESTECH EASYFLOW CANNULA WITH GUIDEWIRE

ESTECH EASYFLOW CANNULA WITH GUIDEWIRE is an FDA 510(k)-cleared medical device (K091542) manufactured by Endoscopic Technologies, Inc. D/B/A Estech. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 19, 2009. Regulation: 8.