510(k) K080169 ยท DXC Clamp, Vascular
HEARTSTRING III PROXIMAL SEAL SYSTEM
| Applicant | Guidant Corporation, Cardiac Surgery, San Jose CA, US |
| Decision | Substantially Equivalent, Feb 8, 2008 |
| Received | Jan 24, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080169
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.