ClearanceBrief
510(k) K262391 ยท NRY Catheter, Thrombus Retriever

APRO 35 Swift Catheter and Alembic Aspiration Tubing

ApplicantAlembic, LLC, Mountain View CA, US
DecisionSubstantially Equivalent, Aug 12, 2026
ReceivedJul 14, 2026
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K262391

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.