510(k) K083040 ยท DCN System, Test, C-Reactive Protein
S-TEST C-REACTIVE PROTEIN (CRP)
| Applicant | Alfa Wassermann Diagnostic Technologies, Inc., West Caldwell NJ, US |
| Decision | Substantially Equivalent, Jan 30, 2009 |
| Received | Oct 14, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083040
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.