510(k) K091952 ยท KRD Device, Vascular, For Promoting Embolization
ACTA VESSEL OCCLUSION SYSTEM (VOS)
| Applicant | Nfocus Neuromedical, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Sep 10, 2010 |
| Received | Jul 1, 2009 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K091952
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.