
Medtrex, Inc.
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O.R.PRO 300 ELECTROSURGICAL GENERATOR MODEL 40001-100 is an FDA 510(k)-cleared medical device (K981724) manufactured by Medtrex, 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 June 21, 1998. Regulation: 8.