Avance Y-Connector S

Avance Y-Connector S is an FDA 510(k)-cleared medical device (K151872) manufactured by Molnlycke Health Care Us, LLC. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 1, 2015. Regulation: 8.