ClearanceBrief
510(k) K232489 ยท IYE Accelerator, Linear, Medical

VenusX

ApplicantLinatech, LLC, Sunnyvale CA, US
DecisionSubstantially Equivalent, Apr 12, 2024
ReceivedAug 17, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232489

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.