MODIFIED CONCENTIRC MICROCATHETER

MODIFIED CONCENTIRC MICROCATHETER is an FDA 510(k)-cleared medical device (K113260) manufactured by Concentric 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 8, 2012. Regulation: 8.