ClearanceBrief
510(k) K854019 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

PORT-GARD

ApplicantCormed, Inc., Sub. C.R.Bard, Inc., Medina NY, US
DecisionSubstantially Equivalent, Nov 26, 1985
ReceivedSep 30, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854019

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.