ClearanceBrief
510(k) K830836 ยท LHI Set, I.V. Fluid Transfer

Q.C. TESTER

ApplicantAlltek Filtration, Inc., Walker MI, US
DecisionSubstantially Equivalent, Apr 18, 1983
ReceivedMar 22, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830836

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.