OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER

OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER is an FDA 510(k)-cleared medical device (K140286) manufactured by Cordis, A Johnson & Johnson Co.. 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 6, 2014. Regulation: 8.