ClearanceBrief
510(k) K002154 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence

K.E.A.T.

ApplicantEmd Electronic Medical Devices, Corp., Miami Beach FL, US
DecisionSubstantially Equivalent, Mar 22, 2001
ReceivedJul 17, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002154

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.