ClearanceBrief
510(k) K180637 ยท HIR Perineometer

leva Pelvic Floor Trainer

ApplicantRenovia, Inc., Boston MA, US
DecisionSubstantially Equivalent, Apr 4, 2018
ReceivedMar 12, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180637

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.