510(k) K012041 ยท DXC Clamp, Vascular
THE HAMMER MODEL H100
| Applicant | Tenacore Holdings, Inc., Mission Viejo, CA, US |
| Decision | Substantially Equivalent, Mar 28, 2002 |
| Received | Jun 29, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012041
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.