510(k) K002056 ยท HCG Device, Neurovascular Embolization
MICRUS MICROCOIL DELIVERY SYSTEM, MDS03
| Applicant | Micrus Corp., Mountain View CA, US |
| Decision | Substantially Equivalent, Jan 11, 2001 |
| Received | Jul 6, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002056
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.