ClearanceBrief
510(k) K212495 ยท HIR Perineometer

Leva Pelvic Health System

ApplicantRenovia, Inc., Boston MA, US
DecisionSubstantially Equivalent, Sep 8, 2021
ReceivedAug 9, 2021
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K212495

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.