NITINOL SEEKER(R) GUIDE WIRES

NITINOL SEEKER(R) GUIDE WIRES is an FDA 510(k)-cleared medical device (K914032) manufactured by Target Therapeutics. 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 10, 1992. Regulation: 8.