ClearanceBrief
510(k) K832079 ยท LIO Device, Specimen Collection

COLLECTION KIT CHLAMYDIA TRACHOMATIS

ApplicantSyva Co., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 29, 1983
ReceivedJun 28, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832079

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.