510(k) K011208 ยท DXC Clamp, Vascular
BIOVER
| Applicant | Biover AG, Ridley Park PA, US |
| Decision | Substantially Equivalent, Oct 2, 2002 |
| Received | Apr 19, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011208
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.