ClearanceBrief
510(k) K964027 ยท LIO Device, Specimen Collection

STP SYSTEM-PVA WITH MERCURY

ApplicantSage Products, Inc., Crystal Lake IL, US
DecisionSubstantially Equivalent, Nov 1, 1996
ReceivedOct 7, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964027

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.