MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA

MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA is an FDA 510(k)-cleared medical device (K920902) 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 May 10, 1993. Regulation: 8.