ClearanceBrief
510(k) K243105 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Ruby Intravascular Catheter

ApplicantVenocare, Inc., Doral FL, US
DecisionSubstantially Equivalent, May 16, 2025
ReceivedSep 30, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K243105

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.