510(k) K800991 ยท DHC System, Test, Systemic Lupus Erythematosus
CORDIA N
| Applicant | Cordis Corp., Walker MI, US |
| Decision | Substantially Equivalent, May 8, 1980 |
| Received | Apr 24, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800991
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.