ClearanceBrief
510(k) K002834 ยท HIR Perineometer

SRS VAGINAL EMG/STIMULATION PERINEOMETER SENSOR SRS ANAL EMG/STIMULATION PERINEOMETER SENSOR

ApplicantSrs Medical Systems, Inc., Redmond WA, US
DecisionSubstantially Equivalent, Nov 29, 2000
ReceivedSep 12, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002834

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.