CLIRPATH TURBO PERIPHERAL CATHETERS

CLIRPATH TURBO PERIPHERAL CATHETERS is an FDA 510(k)-cleared medical device (K060012) manufactured by Spectranetics 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 28, 2006. Regulation: 8.