ClearanceBrief
510(k) K092149 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

BOSS COAGULATION DEVICE, MODEL BOSS1215, BOSS COAGULATION DEVICE, ANGLED ACCESS, MODEL BOSA1215

ApplicantBovie Medical, Clearwater FL, US
DecisionSubstantially Equivalent, Mar 18, 2010
ReceivedJul 16, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092149

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.