510(k) K951314 ยท HCG Device, Neurovascular Embolization
TRUEFILL PVA PARTICLES
| Applicant | Cordis Neurovascular, Inc., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Aug 8, 1995 |
| Received | Mar 23, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951314
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.