ClearanceBrief
510(k) K210406 ยท KGE Forceps, Biopsy, Electric

Bipolar Coagulation Foreceps

ApplicantHangzhou AGS MedTech Co., Ltd., Hangzhou, CN
DecisionSubstantially Equivalent, Oct 5, 2021
ReceivedFeb 10, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K210406

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.