510(k) K250276 ยท KRD Device, Vascular, For Promoting Embolization
Nitinol Enhanced Device (NED)
| Applicant | Embolization, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, May 15, 2025 |
| Received | Jan 31, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250276
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.