
Connexall USA, Inc.
Free shipping on orders over $99 · 30-day returns
CONNEXALL SUITE OF SOFTWARE PRODUCTS is an FDA 510(k)-cleared medical device (K112650) manufactured by Connexall USA, 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 January 31, 2012. Regulation: 8.