
Ambu A/S
Free shipping on orders over $99 · 30-day returns
AMBU OVAL SILICONE RESUSCITATOR, ADULT AND PEDIATRIC is an FDA 510(k)-cleared medical device (K102824) manufactured by Ambu A/S. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 27, 2011. Regulation: 8.