ClearanceBrief
510(k) K904077 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

VITAL-PORT DUAL LUMEN VASCULAR ACCESS SYSTEM

ApplicantMed Institute, Inc., West Lafayette IN, US
DecisionSubstantially Equivalent, Oct 17, 1990
ReceivedSep 5, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904077

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.