510(k) K100454 ยท HCG Device, Neurovascular Embolization
HYDROCOIL EMBOLIC SYSTEM-HYDROFRAME MODEL 100931HFM-V, 101243HFM-V, 180827HFM-V, 181139HFM-V, 181445HFM-V, 181850HFM-V
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Apr 22, 2010 |
| Received | Feb 17, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100454
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.