
Mentor O & O, Inc.
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MENTOR(R) WET-FIELD(R) II AC COAGULATOR, 22-1305 is an FDA 510(k)-cleared medical device (K911160) manufactured by Mentor O & O, 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 May 1, 1991. Regulation: 8.