510(k) K123041 ยท DXC Clamp, Vascular
VASOSTAT HEMOSTASIS DEVICE
| Applicant | Forge Medical, Inc., Wayne NJ, US |
| Decision | Substantially Equivalent, May 29, 2013 |
| Received | Sep 28, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123041
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.