
Estech, Inc.
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ESTECH COBRA(R) GENESIS BIPOLAR CLAMP is an FDA 510(k)-cleared medical device (K133017) manufactured by Estech, Inc.. 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 October 6, 2013. Regulation: 8.