ClearanceBrief
510(k) K222388 ยท NEY System, Ablation, Microwave And Accessories

swiftPro System

ApplicantEmblation , Ltd., Alloa, GB
DecisionSubstantially Equivalent, May 4, 2023
ReceivedAug 8, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222388

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.