CLIRPATH TURBO EXCIMER LASER CATHETERS

CLIRPATH TURBO EXCIMER LASER CATHETERS is an FDA 510(k)-cleared medical device (K052296) 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 1, 2005. Regulation: 8.