ClearanceBrief
510(k) K260916 · LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

FLEXI-PORT™ Power Injectable Implantable Port

ApplicantPortal Access, Inc., Miami Beach FL, US
DecisionSubstantially Equivalent, Jun 17, 2026
ReceivedMar 19, 2026
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K260916

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.