
Olympus America, Inc.
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OLYMPUS UES-20 ELECTROSURGICAL SYSTEM AND ITS ASSOCIATED ACCESSORIES is an FDA 510(k)-cleared medical device (K970184) manufactured by Olympus America, 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 April 10, 1997. Regulation: 8.