ClearanceBrief
510(k) K200146 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

HET Bipolar Electrocautery Forceps, HET Bipolar Electrocautery Monitor

ApplicantCovidien, LLC, Mansfield MA, US
DecisionSubstantially Equivalent, May 7, 2020
ReceivedJan 22, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K200146

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.