
Digirad Corp.
Free shipping on orders over $99 · 30-day returns
CARDIUS 3 X-ACT is an FDA 510(k)-cleared medical device (K083649) manufactured by Digirad Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 8, 2009. Regulation: 8.