510(k) K133029 ยท DXC Clamp, Vascular
ABDOMINAL AORTIC AND JUNCTIONAL TOURNIQUET (AAJT) DEVICE
| Applicant | Compression Works, LLC, Providence RI, US |
| Decision | Substantially Equivalent, Dec 6, 2013 |
| Received | Sep 26, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133029
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.