STEREOTAXIS ENDOVASCULAR GUIDE WIRE

STEREOTAXIS ENDOVASCULAR GUIDE WIRE is an FDA 510(k)-cleared medical device (K042854) manufactured by Stereotaxis, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 7, 2005. Regulation: 8.