ClearanceBrief
510(k) K082568 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

SALINE ENHANCED ELECTROSURGICAL RESECTION (SEER) DEVICE

ApplicantBovie Medical, St. Petersburg FL, US
DecisionSubstantially Equivalent, Nov 17, 2008
ReceivedSep 4, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082568

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.