ClearanceBrief
510(k) K151963 ยท LHI Set, I.V. Fluid Transfer

SmartSite Vented Vial Access Device

ApplicantYukon Medical, LLC, Durham NC, US
DecisionSubstantially Equivalent, Jul 31, 2015
ReceivedJul 16, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K151963

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.