510(k) K980631 ยท DXC Clamp, Vascular
EMBOL-X AORTIC OCCLUSION AND CARDIOPLEGIA CANNULA
| Applicant | Embol-X, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Feb 2, 1999 |
| Received | Feb 18, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980631
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.