510(k) K931409 ยท CGR Radioimmunoassay, Cortisol
IMMULITE CORTISOL
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, May 11, 1993 |
| Received | Mar 19, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931409
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 23, 2014 | Siemens Healthcare Diagnostics IMMULITE /IMMULITE 1000 Systems COR Cortisol, REF/Catalog Number LKC01, SMN 10381388, IVD.
For in vitro diagnostic use with the IMMULITE 1000 Systems Analyzers for the quantitative measurement measur Terminated |
CGR | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.