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Bovie Medical
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SALINE ENHANCED ELECTROSURGICAL RESECTION (SEER) DEVICE is an FDA 510(k)-cleared medical device (K082568) manufactured by Bovie Medical. 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 November 16, 2008. Regulation: 8.