LEAD STYLET,MODELS 6505,6506,6507,6508

LEAD STYLET,MODELS 6505,6506,6507,6508 is an FDA 510(k)-cleared medical device (K992863) manufactured by Guidant 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 November 11, 1999. Regulation: 8.