510(k) K012145 ยท HCG Device, Neurovascular Embolization
MICROPLEX COIL SYSTEM
| Applicant | MicroVention, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Oct 29, 2001 |
| Received | Jul 10, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012145
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.