ClearanceBrief
510(k) K253590 ยท NRY Catheter, Thrombus Retriever

Millipede System

ApplicantPerfuze, Ltd., Galway, IE
DecisionSubstantially Equivalent, Mar 16, 2026
ReceivedNov 17, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K253590

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.