ClearanceBrief
510(k) K830972 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

I.V. CATHETER PLACEMENT UNIT POLYURETH

ApplicantCritikon Company, LLC, Walker MI, US
DecisionSubstantially Equivalent, Apr 27, 1983
ReceivedMar 28, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830972

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.