RENEGADE HI-FLO MICROCATHETER

RENEGADE HI-FLO MICROCATHETER is an FDA 510(k)-cleared medical device (K000177) manufactured by Boston Scientific Corp. 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 6, 2000. Regulation: 8.