ClearanceBrief
510(k) K960051 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

NIPRO SAFELET CATH

ApplicantNissho Corp., Lexington KY, US
DecisionSubstantially Equivalent, Mar 28, 1996
ReceivedJan 4, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960051

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.