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AtriCure, Inc.
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ATRICURE CRYO1 CRYO-ABLATION PROBE is an FDA 510(k)-cleared medical device (K082074) manufactured by AtriCure, Inc.. 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 March 1, 2009. Regulation: 8.