BAXTER SENSOR CORONARY GUIDEWIRE

BAXTER SENSOR CORONARY GUIDEWIRE is an FDA 510(k)-cleared medical device (K923240) 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 September 22, 1992. Regulation: 8.