510(k) K942328 ยท DHR System, Test, Rheumatoid Factor
N LATEX RF
| Applicant | Behring Diagnostics, Inc., Westwood MA, US |
| Decision | Substantially Equivalent, Oct 20, 1994 |
| Received | May 5, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942328
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.