ClearanceBrief
510(k) K182451 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

BiZact Tonsillectomy Device Advanced Bipolar Tissue Sealer/Divider

ApplicantCovidien, LLC, Boulder CO, US
DecisionSubstantially Equivalent, Nov 6, 2018
ReceivedSep 7, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182451

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.