ClearanceBrief
510(k) K922562 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence

STIMTECH PFX, CATALOG NUMBER 78-8540

ApplicantStimtech Products, Marlborough MA, US
DecisionSubstantially Equivalent, Oct 13, 1993
ReceivedJun 1, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922562

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.