510(k) K033813 ยท HCG Device, Neurovascular Embolization
MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTE
| Applicant | Micrus Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Feb 4, 2004 |
| Received | Dec 9, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033813
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.