ClearanceBrief
510(k) K970145 ยท HIR Perineometer

PERINEOMETER & VAGINAL PROBE (BIOFEEDBACK MONITOR #20 AND VAGINAL PROBE)

ApplicantBiosearch Medical Products, Inc., Somerville NJ, US
DecisionSubstantially Equivalent, Aug 11, 1997
ReceivedJan 15, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970145

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.