STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO

STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO is an FDA 510(k)-cleared medical device (K122960) manufactured by Oscor, 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 December 12, 2012. Regulation: 8.