ClearanceBrief
510(k) K170777 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Bovie J-Plasma Precise FLEX Handpiece

ApplicantBovie Medical Corporation, Clearwater FL, US
DecisionSubstantially Equivalent, May 1, 2017
ReceivedMar 15, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170777

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.