510(k) K250492 ยท DQY Catheter, Percutaneous
FlexiGo 3D Delivery Catheter
| Applicant | CenterPoint Systems, LLC, West Valley City UT, US |
| Decision | Substantially Equivalent, Jun 18, 2025 |
| Received | Feb 20, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K250492
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.