510(k) K192413 ยท DXC Clamp, Vascular
SiteSeal Femoral Compression Device
| Applicant | Ensite Vacular, LLC, Olathe KS, US |
| Decision | Substantially Equivalent, Mar 31, 2020 |
| Received | Sep 4, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192413
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.