510(k) K033372 ยท HCG Device, Neurovascular Embolization
SAPPHIRE DETACHABLE FIBERED COIL SYSTEM, HELIX FIBERED, CYCLONE, MULTIPLE MODELS
| Applicant | Micro Therapeutics, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 9, 2004 |
| Received | Oct 22, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033372
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.