
Cordis Neurovascular, Inc.
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HYPERTRANSIT INFUSION CATHETER is an FDA 510(k)-cleared medical device (K043538) 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 April 17, 2005. Regulation: 8.