ClearanceBrief
510(k) K823838 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

INFUSE-A-PORT

ApplicantInfusaid Corp., Walker MI, US
DecisionSubstantially Equivalent, Jan 12, 1983
ReceivedDec 28, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823838

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.