ClearanceBrief
510(k) K955839 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER

ApplicantBaxter Edwards, Irvine CA, US
DecisionSubstantially Equivalent, Mar 25, 1996
ReceivedDec 26, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955839

DateFirm and productCodeLinked 510(k)
Dec 2, 2016Centurion Medical Products Corporation
Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The Multi-Med catheter is indicated for use in patients requiring administration of solutions, blood sampling, and central venous p
Terminated
FOZNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.