510(k) K133237 ยท KRD Device, Vascular, For Promoting Embolization
GEL-BEAD EMBOLIZATION SPHERES
| Applicant | Vascular Solutions, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 25, 2014 |
| Received | Oct 21, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133237
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.