SARNS VISIFLOW AORTIC ARCH CANNULA

SARNS VISIFLOW AORTIC ARCH CANNULA is an FDA 510(k)-cleared medical device (K874896) manufactured by 3M Health Care, Sarns. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 1, 1988. Regulation: 8.