BAXTER TREK *14 INTERMEDIATE AND SUPPORT GUIDEWIRES

BAXTER TREK *14 INTERMEDIATE AND SUPPORT GUIDEWIRES is an FDA 510(k)-cleared medical device (K951307) manufactured by Baxter Healthcare 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 June 21, 1995. Regulation: 8.