510(k) K983483 ยท HCG Device, Neurovascular Embolization
VASCULAR OCCLUSION SYSTEM
| Applicant | Cordis Neurovascular, Inc., Miami Lake FL, US |
| Decision | Substantially Equivalent, Mar 24, 1999 |
| Received | Oct 5, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983483
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.