510(k) K071939 ยท KRD Device, Vascular, For Promoting Embolization
HYDROCOIL EMBOLIC SYSTEMS (HES)
| Applicant | MicroVention, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Jan 11, 2008 |
| Received | Jul 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071939
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.