
Guidant Corporation, Cardiac Surgery
Free shipping on orders over $99 · 30-day returns
GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM is an FDA 510(k)-cleared medical device (K024071) manufactured by Guidant Corporation, Cardiac Surgery. 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 13, 2003. Regulation: 8.