ClearanceBrief
510(k) K802075 ยท FKI Set, Dialyzer Holder

HOLLOW FIBER DIALYZER HOLDER

ApplicantRenal Devices, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 16, 1980
ReceivedAug 27, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802075

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.