ClearanceBrief
510(k) K912465 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

VITAL-PORT DUAL LUMEN VASCULAR ACCESS SYSTEM 1121

ApplicantMed Institute, Inc., West Lafayette IN, US
DecisionSubstantially Equivalent, Jul 30, 1991
ReceivedJun 4, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912465

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.