
Ncontact Surgical, Inc.
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NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021;CSK-022; CSK-023; CSK-025 is an FDA 510(k)-cleared medical device (K082203) manufactured by Ncontact Surgical, 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 December 29, 2008. Regulation: 8.