510(k) K233948 · OBJ Catheter, Ultrasound, Intravascular
Provisio SLT IVUS System
| Applicant | Provisio Medical, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Apr 23, 2024 |
| Received | Dec 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233948
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.