LASSO NAV DUO LOOP CATHETER

LASSO NAV DUO LOOP CATHETER is an FDA 510(k)-cleared medical device (K130602) manufactured by Biosense Webster, 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 August 13, 2013. Regulation: 8.