EVI SUTURED-CLIP APPLIER

EVI SUTURED-CLIP APPLIER is an FDA 510(k)-cleared medical device (K971588) manufactured by Elective Vascular Intervention Inc. (Evi). 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 23, 1997. Regulation: 8.