ClearanceBrief
510(k) K211000 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ACUTRON

ApplicantIlooda Co,., Ltd., Suwon-Si, KR
DecisionSubstantially Equivalent, Jun 9, 2022
ReceivedApr 2, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K211000

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.