ClearanceBrief
510(k) K771375 ยท FKQ System, Dialysate Delivery, Central Multiple Patient

PRESSURE MODULE 5M1247

ApplicantTravenol Laboratories, S.A., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 15, 1977
ReceivedJul 25, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K771375

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.