ClearanceBrief
510(k) K782083 ยท HIR Perineometer

VAGATEX

ApplicantVagatex, Mchenry IL, US
DecisionSubstantially Equivalent, Jan 3, 1979
ReceivedDec 14, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K782083

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.