510(k) K063057 ยท NQD Cardiac C-Reactive Protein, Antigen, Antiserum, And Control
IMMULITE/IMMULITE 1000, IMMULITE 2000 HIGH SENSITIVITY CRP
| Applicant | Diagnostic Products Corporation, Los Angeles CA, US |
| Decision | Substantially Equivalent, Dec 22, 2006 |
| Received | Oct 5, 2006 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K063057
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.