ClearanceBrief
510(k) K870817 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

MEDIPORT II MODEL MP-DL VASCULAR ACCESS PORT

ApplicantC.R. Bard, Inc., Murray Hill NJ, US
DecisionSubstantially Equivalent, Jul 30, 1987
ReceivedMar 3, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870817

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.