510(k) K032872 ยท HCG Device, Neurovascular Embolization
MICRUS MICROCOIL SYSTEM
| Applicant | Micrus Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Nov 28, 2003 |
| Received | Sep 15, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032872
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.