ClearanceBrief
510(k) K964048 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

FIRST MIDCATH CATHETER KIT

ApplicantBecton Dickinson Vascular Access, Inc., Sandy UT, US
DecisionSubstantially Equivalent, Jan 6, 1997
ReceivedOct 9, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964048

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.