REMOVE LABELING RESTRICT FROM GUIDE WIRES

REMOVE LABELING RESTRICT FROM GUIDE WIRES is an FDA 510(k)-cleared medical device (K912293) 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 December 4, 1991. Regulation: 8.