510(k) K003372 ยท DCN System, Test, C-Reactive Protein
IMMULITE HIGH SENSITIVITY CRP, IMMULITE 2000 HIGH SENSITIVITY CRP
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Dec 26, 2000 |
| Received | Oct 30, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003372
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.