ClearanceBrief
510(k) K031282 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

OPTILOCK IMPLANTABLE ACCESS PORT, MODEL 1700-05

ApplicantLeMaitre Vascular, Inc., Burlington MA, US
DecisionSubstantially Equivalent, Aug 5, 2003
ReceivedApr 22, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031282

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.