ClearanceBrief
510(k) K150514 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

Power-Injectable Implantable Ports with ChronoFlex Polyurethane Catheters

ApplicantC.R. Bard, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Nov 20, 2015
ReceivedFeb 27, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K150514

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.