ClearanceBrief
510(k) K192807 ยท MPB Catheter, Hemodialysis, Non-Implanted

Duo-Flow Side x Side Double Lumen Catheter

ApplicantMedical Components, Inc. (dba MedComp), Harleysville PA, US
DecisionSubstantially Equivalent, Apr 23, 2020
ReceivedOct 1, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192807

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.