ClearanceBrief
510(k) K863305 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

HICKMAN SUBCUTANEOUS PORT W/PRE-ATTACHED CATHETER

ApplicantC.R. Bard, Inc., Murray Hill NJ, US
DecisionSubstantially Equivalent, Oct 10, 1986
ReceivedAug 25, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863305

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.