510(k) K092503 ยท DXC Clamp, Vascular
RADAR VASCULAR COMPRESSION DEVICES
| Applicant | Advanced Vascular Dynamics, Portland OR, US |
| Decision | Substantially Equivalent, Nov 19, 2009 |
| Received | Aug 14, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092503
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.