510(k) K021608 ยท DXC Clamp, Vascular
SMITHWICK CAROTID SHUNT
| Applicant | Implantable Devices, Tampa FL, US |
| Decision | Substantially Equivalent, Oct 22, 2002 |
| Received | May 16, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021608
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.