510(k) K062182 ยท DLJ Calibrators, Drug Specific
DIMENSION VISTA SYSTEM ECSTASY CALIBRATOR, MODEL KC520
| Applicant | Dade Behring, Inc., Newark DE, US |
| Decision | Substantially Equivalent, Sep 14, 2006 |
| Received | Jul 31, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062182
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.