510(k) K903852 ยท DHR System, Test, Rheumatoid Factor
RAPITEX(R) RF NEW
| Applicant | Behring Diagnostics, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, Aug 30, 1990 |
| Received | Aug 21, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903852
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.