ClearanceBrief
510(k) K242588 ยท DQY Catheter, Percutaneous

COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL)

ApplicantOrbusNeich Medical (Shenzhen) Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Jan 7, 2025
ReceivedAug 30, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242588

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.