ClearanceBrief
510(k) K790105 ยท GKT Separator, Automated, Blood Cell, Diagnostic

TERUMO IMUGARD

ApplicantTerumo America, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 24, 1979
ReceivedJan 16, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790105

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.