510(k) K082324 ยท HCG Device, Neurovascular Embolization
TRUFILL DCS SYRINGE
| Applicant | Cordis Neurovascular, Inc., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Sep 12, 2008 |
| Received | Aug 14, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082324
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.