510(k) K093813 ยท KRD Device, Vascular, For Promoting Embolization
OCCLUSIN 500 ARTIFICIAL EMBOLIZATION DEVICE
| Applicant | Imbiotechnologies, North Attleboro MA, US |
| Decision | Substantially Equivalent, May 10, 2010 |
| Received | Dec 11, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093813
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.