ClearanceBrief
510(k) K220138 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Surtron 80 D, Surtron 160, Surtron 200, Surtron Flash 160 HF, Surtron 400 HP

ApplicantLed Spa, Aprilia, IT
DecisionSubstantially Equivalent, Oct 5, 2022
ReceivedJan 18, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220138

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.