RX VIATRAC 14 PERIPHERAL DILATATION CATHETER

RX VIATRAC 14 PERIPHERAL DILATATION CATHETER is an FDA 510(k)-cleared medical device (K000101) 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 February 9, 2000. Regulation: 8.