510(k) K984214 ยท DXC Clamp, Vascular
CORDIS ENDOVASCULAR TEMPORARY OCCLUSION BALLOON CATHETER
| Applicant | Cordis Neurovascular, Inc., Miami Lake FL, US |
| Decision | Substantially Equivalent, Aug 10, 1999 |
| Received | Nov 24, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984214
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.