ClearanceBrief
510(k) K221476 ยท HIR Perineometer

Perifit

ApplicantX6 Innovations, Paris, FR
DecisionSubstantially Equivalent, Feb 10, 2023
ReceivedMay 20, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221476

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.