ClearanceBrief
510(k) K221672 ยท NEY System, Ablation, Microwave And Accessories

Creo Electrosurgical System with NP1 Instrument

ApplicantCreo Medical, Ltd., Chepstow, GB
DecisionSubstantially Equivalent, Feb 14, 2023
ReceivedJun 9, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221672

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.