ClearanceBrief
510(k) K864349 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

MEDIPORT II SINGLE LUM/PORT IMPLANT VASC ACS PORT

ApplicantC.R. Bard, Inc., Murray Hill NJ, US
DecisionSubstantially Equivalent, Feb 10, 1987
ReceivedNov 4, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864349

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.