510(k) K080437 ยท HCG Device, Neurovascular Embolization
MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 CERECYTE, MODEL CDF
| Applicant | Micrus Endovascular Corporation, San Jose CA, US |
| Decision | Substantially Equivalent, May 8, 2008 |
| Received | Feb 15, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080437
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.