ClearanceBrief
510(k) K801559 ยท FJI Dialyzer, Capillary, Hollow Fiber

HOLLO FIBER DIALYZER

ApplicantRenal Devices, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 31, 1980
ReceivedJul 8, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801559

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.