ClearanceBrief
510(k) K232945 · NIE Catheter, Hemodialysis, Triple Lumen, Non-Implanted

Trio-CT­® Triple Lumen Catheter w/ Curved Extensions

ApplicantMedical Components, Inc. (dba MedComp), Harleysville PA, US
DecisionUnknown, Nov 16, 2023
ReceivedSep 20, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232945

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.