ClearanceBrief
510(k) K930530 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence

INCARE PRS 9300 PELVIC FL THERA SYST/TREAT URI INC

ApplicantHollister, Inc., Libertyville IL, US
DecisionSubstantially Equivalent, Oct 17, 1995
ReceivedFeb 2, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930530

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.