510(k) K850296 ยท DHR System, Test, Rheumatoid Factor
LASER RF TEST -RHEUMATOID FACTOR(S) REAGENTS
| Applicant | Behring Diagnostics, Inc., La Jolla CA, US |
| Decision | Substantially Equivalent, Apr 12, 1985 |
| Received | Jan 24, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850296
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.