ClearanceBrief
510(k) K251014 ยท DQY Catheter, Percutaneous

APRO 45 Catheter

ApplicantAlembic, LLC, Mountain View CA, US
DecisionSubstantially Equivalent, May 1, 2025
ReceivedApr 2, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K251014

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.