VERIPATH PERIPHERAL GUIDING CATHETER

VERIPATH PERIPHERAL GUIDING CATHETER is an FDA 510(k)-cleared medical device (K994229) manufactured by Advanced Cardiovascular Systems, 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 February 24, 2000. Regulation: 8.