ClearanceBrief
510(k) K842075 ยท FPB Filter, Infusion Line

CRITIKON I.V. FILTER

ApplicantCritikon Company, LLC, Mchenry IL, US
DecisionSubstantially Equivalent, Jun 28, 1984
ReceivedMay 23, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842075

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.