
Cryo Vascular Systems, Inc.
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POLARCATH PERIPHERAL DILATATION SYSTEM is an FDA 510(k)-cleared medical device (K033622) manufactured by Cryo Vascular Systems, Inc.. 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 9, 2004. Regulation: 8.