510(k) K233858 ยท DQY Catheter, Percutaneous
TriSalus TriGuideTM Guiding Catheter
| Applicant | Trisalus Life Sciences, Westminster CO, US |
| Decision | Substantially Equivalent, Dec 27, 2023 |
| Received | Dec 5, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233858
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.