510(k) K112181 ยท HCG Device, Neurovascular Embolization
HYDROCOIL(R) EMBOLIC SYSTEM (HES)
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Dec 1, 2011 |
| Received | Jul 28, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112181
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.