ClearanceBrief
510(k) K093600 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence

OMNISTIM CONTINENCE+ PELVIC FLOOR STIMULATION SYSTEM

ApplicantAccelerated Care Plus, Reno NV, US
DecisionSubstantially Equivalent, Dec 4, 2009
ReceivedNov 20, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093600

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.