ClearanceBrief
510(k) K032044 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

X-PROT DUO PORT

ApplicantC.R. Bard, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Jul 10, 2003
ReceivedJul 2, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K032044

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.