
Cordis Corp.
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CORDIS AMIIA .014 PTA BALLOON CATHETER is an FDA 510(k)-cleared medical device (K050645) manufactured by Cordis Corp.. 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 31, 2005. Regulation: 8.