ClearanceBrief
510(k) K001795 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

THE AVITRO LLC, 10 AND 100 USO UNITS/ML HEPARIN SODIUM VAFD

ApplicantAvitro, LLC, Woodstock IL, US
DecisionSubstantially Equivalent, Oct 19, 2000
ReceivedJun 14, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001795

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.