BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH

BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH is an FDA 510(k)-cleared medical device (K911367) 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 9, 1991. Regulation: 8.