510(k) K133924 ยท KRD Device, Vascular, For Promoting Embolization
ENDOLUMINAL OCCLUSION SYSTEM (EOS)
| Applicant | Artventive Medical Group, Inc., Woodinville WA, US |
| Decision | Substantially Equivalent, Dec 3, 2014 |
| Received | Dec 23, 2013 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K133924
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.