510(k) K801961 ยท DHR System, Test, Rheumatoid Factor
RF-II TEST KIT
| Applicant | Immuno-Diagnostic Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 10, 1980 |
| Received | Aug 19, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801961
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.