510(k) K083896 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
DESTINY MAX COAGULATION ANALYZER
| Applicant | Trinity Biotech, Jamestown NY, US |
| Decision | Substantially Equivalent, Jul 2, 2009 |
| Received | Dec 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083896
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.