510(k) K150402 ยท KRD Device, Vascular, For Promoting Embolization
Endoluminal Occlusion System-EOS
| Applicant | Artventive Medical Group, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Sep 25, 2015 |
| Received | Feb 18, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150402
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.