ClearanceBrief
510(k) K983052 ยท HIR Perineometer

PERITRON PERINEOMETER MODEL 9300V OR 9300A

ApplicantCardio Design Pty. , Ltd., Baulkham Hills Nsw, AU
DecisionSubstantially Equivalent, Oct 19, 1998
ReceivedSep 1, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983052

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.