
Cameron-Miller, Inc.
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ELECTROSURGICAL DEVICE, MODEL 26-2500 is an FDA 510(k)-cleared medical device (K935490) manufactured by Cameron-Miller, 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 March 31, 1994. Regulation: 8.