510(k) K043371 ยท KRD Device, Vascular, For Promoting Embolization
BIOMERIX VASCULAR OCCLUSION DEVICE AND LOADER
| Applicant | Biomerix Corporation, Rockville MD, US |
| Decision | Substantially Equivalent, Feb 3, 2005 |
| Received | Dec 8, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043371
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.