
Trans Vascular Incorporated
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CROSSPOINT TRANSACCESS CATHETER, MODEL TA-XP-001 is an FDA 510(k)-cleared medical device (K031920) manufactured by Trans Vascular Incorporated. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 22, 2003. Regulation: 8.