510(k) K030182 ยท GGN Plasma, Coagulation Control
LIQUICHEK D-DIMER CONTROL, MODEL 356, 357
| Applicant | Bio-Rad, Irvine CA, US |
| Decision | Substantially Equivalent, Feb 24, 2003 |
| Received | Jan 17, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030182
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.