510(k) K162027 ยท DXC Clamp, Vascular
TRAcelet Compression Device
| Applicant | Medtronic Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Oct 21, 2016 |
| Received | Jul 22, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162027
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.