ClearanceBrief
510(k) K250772 ยท NLH Catheter, Recording, Electrode, Reprocessed

Medline ReNewal Reprocessed Boston Scientific Dynamic XT Unidirectional Steerable Diagnostic Catheter

ApplicantSurgical Instrument Service and Savings, Inc., Redmond OR, US
DecisionSubstantially Equivalent, Jul 11, 2025
ReceivedMar 13, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K250772

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.