
Stereotaxis, Inc.
Free shipping on orders over $99 · 30-day returns
CRONUS GUIDEWIRE, MODEL 001-001470-1 is an FDA 510(k)-cleared medical device (K051373) 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 December 8, 2005. Regulation: 8.