510(k) K790012 ยท DHR System, Test, Rheumatoid Factor
RHEUMOGEN TEST SYSTEM
| Applicant | Calbiochem-Behring Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 26, 1979 |
| Received | Jan 2, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790012
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.