510(k) K080069 ยท DAP Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control
DIMERTEST
| Applicant | American Diagnostica, Inc., Stamford CT, US |
| Decision | Substantially Equivalent, Feb 13, 2008 |
| Received | Jan 10, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080069
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.