VIA MICROCATHETER, VIA PLUS MICROCATHETER

VIA MICROCATHETER, VIA PLUS MICROCATHETER is an FDA 510(k)-cleared medical device (K123477) manufactured by Sequent Medical, 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 March 18, 2013. Regulation: 8.