ClearanceBrief
510(k) K791106 ยท GKT Separator, Automated, Blood Cell, Diagnostic

STERILE, DISPOSABLE CENTRIFUGE BOWL

ApplicantTravenol Laboratories, S.A., Walker MI, US
DecisionSubstantially Equivalent, Aug 10, 1979
ReceivedJun 13, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791106

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.