ClearanceBrief
510(k) K223138 ยท NEY System, Ablation, Microwave And Accessories

AB1 Electrosurgical Instrument, Creo Electrosurgical System

ApplicantCreo Medical, Ltd., Chepstow, UA
DecisionSubstantially Equivalent, Jun 26, 2023
ReceivedOct 4, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223138

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.