ClearanceBrief
510(k) K160539 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

BiZact Open Sealer/Divider

ApplicantCovidien, Boulder CO, US
DecisionSubstantially Equivalent, Jun 15, 2016
ReceivedFeb 26, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160539

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.