510(k) K851537 ยท DHR System, Test, Rheumatoid Factor
LASER RF CONTROL SERUM-QUALITY CONTROL SERUM
| Applicant | Behring Diagnostics, Inc., La Jolla CA, US |
| Decision | Substantially Equivalent, Jun 5, 1985 |
| Received | Apr 16, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851537
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.