ClearanceBrief
510(k) K242337 ยท DQY Catheter, Percutaneous

FlowGuide (FG60F); GuidionShort (GS60F)

ApplicantImds Operations B.V., Roden, NL
DecisionSubstantially Equivalent, Apr 17, 2025
ReceivedAug 7, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242337

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.