ClearanceBrief
510(k) K222679 ยท KRA Catheter, Continuous Flush

Vericor Support Catheter

ApplicantVascupatent Medical (Shenzhen) Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Nov 7, 2022
ReceivedSep 6, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222679

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.