510(k) K103008 ยท HCG Device, Neurovascular Embolization
INZONE DETACHMENT SYSTEM
| Applicant | Boston Scientific Corp, Fremont CA, US |
| Decision | Substantially Equivalent, Dec 10, 2010 |
| Received | Oct 12, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103008
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.