ClearanceBrief
510(k) K231780 ยท HIR Perineometer

Perifit Care+

ApplicantX6 Innovations, Paris, FR
DecisionSubstantially Equivalent, Dec 20, 2023
ReceivedJun 16, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231780

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.