ClearanceBrief
510(k) K200293 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence

InMode System with vTone Applicator

ApplicantInMode , Ltd., Yokneam, IL
DecisionSubstantially Equivalent, May 5, 2020
ReceivedFeb 5, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K200293

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.