Reliance® Fusion Sterilization Wraps

Reliance® Fusion Sterilization Wraps is an FDA 510(k)-cleared medical device (K230137) manufactured by Ahlstrom-Munksjo Nonwovens, LLC. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 6, 2023. Regulation: 8.