
Vascular Solutions, Inc.
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TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230 is an FDA 510(k)-cleared medical device (K062877) manufactured by Vascular Solutions, 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 January 17, 2007. Regulation: 8.