510(k) K071247 ยท DHR System, Test, Rheumatoid Factor
N LATEX RF KIT
| Applicant | Dade Behring, Inc., Newark DE, US |
| Decision | Substantially Equivalent, Aug 8, 2007 |
| Received | May 4, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071247
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.