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Cordis Corp., A Johnson & Johnson Co.
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OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETER is an FDA 510(k)-cleared medical device (K091077) manufactured by Cordis Corp., 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 February 3, 2010. Regulation: 8.