510(k) K041551 ยท HCG Device, Neurovascular Embolization
MODIFICATION TO: HYDROCOIL EMBOLIC SYSTEM (HES)
| Applicant | MicroVention, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Jul 7, 2004 |
| Received | Jun 9, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041551
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.