
Weck
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WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER is an FDA 510(k)-cleared medical device (K021808) manufactured by Weck. 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 August 13, 2002. Regulation: 8.