ClearanceBrief
510(k) K190559 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

SmartPort+ Implantable Ports, SmartPort Plastic Implantable Ports

ApplicantAngioDynamics, Inc., Marlborough MA, US
DecisionSubstantially Equivalent, May 22, 2020
ReceivedMar 5, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190559

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.