ClearanceBrief
510(k) K990041 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence

UROSTYM BIOFEEDBACK AND STIMULATION PROBES

ApplicantLaborie Medical Tech Corp., Williston VT, US
DecisionSubstantially Equivalent, Aug 5, 1999
ReceivedJan 6, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990041

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.