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Guidant Corporation, Cardiac Surgery
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GUIDANT MICROWAVE ABLATION SYSTEM is an FDA 510(k)-cleared medical device (K041340) manufactured by Guidant Corporation, Cardiac Surgery. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 27, 2004. Regulation: 8.