510(k) K792061 ยท DHR System, Test, Rheumatoid Factor
CORDIA RF
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 27, 1979 |
| Received | Oct 15, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792061
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.