510(k) K831941 ยท DHR System, Test, Rheumatoid Factor
LEAP RHEUMATOID FACTOR TEST KIT
| Applicant | Cooper Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 18, 1983 |
| Received | Jun 16, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831941
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.