VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER

VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER is an FDA 510(k)-cleared medical device (K012050) manufactured by Guidant Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 5, 2001. Regulation: 8.