ClearanceBrief
510(k) K893460 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

A-PORT IMPLANT VASCULAR ACCESS SYSTEM .6MM/2.29MM

ApplicantTherex Corp., Walpole MA, US
DecisionSubstantially Equivalent, Jun 23, 1989
ReceivedMay 3, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893460

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.