510(k) K070323 ยท DXC Clamp, Vascular
TEMPORARY LIMB SALVAGE SHUNT
| Applicant | Vascutek, Ltd., Renfrewshire, Glasgow, GB |
| Decision | Substantially Equivalent, Feb 15, 2007 |
| Received | Feb 2, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070323
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.