510(k) K904497 ยท DCN System, Test, C-Reactive Protein
CROMATEST RHEUMATOID DIAGNOSTIC/CRP LATEX TEST
| Applicant | Biotrax, Inc., Baltimore MD, US |
| Decision | Substantially Equivalent, Nov 1, 1990 |
| Received | Oct 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904497
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.