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Cordis Neurovascular, Inc.
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PROWLER SELECT 10 AND 14 INFUSION CATHETERS WITH AND WITHOUT PRE-SHAPED TIPS is an FDA 510(k)-cleared medical device (K020680) manufactured by Cordis Neurovascular, 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 March 26, 2002. Regulation: 8.