
Covidien
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Premium Surgiclip¿; Endo Clip¿; AcuClip¿ is an FDA 510(k)-cleared medical device (K143644) manufactured by Covidien. 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 September 13, 2015. Regulation: 8.