ClearanceBrief
510(k) K231126 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Eblator Device

ApplicantE Surgical, LLC, Sparks NV, US
DecisionSubstantially Equivalent, Aug 2, 2023
ReceivedApr 20, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231126

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.