ClearanceBrief
510(k) K021580 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

OPTILOCK IMPLANTABLE ACCESS PORT, MODELS #1700-01, 1700-02, 1700-03, 1700-04 AND 1700-05

ApplicantLeMaitre Vascular, Inc., Burlington MA, US
DecisionSubstantially Equivalent, Feb 12, 2003
ReceivedMay 14, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021580

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.