510(k) K892051 ยท LFX Enzyme Linked Immunoabsorbent Assay, Rubella
RUBELLA-CUBE(TM)
| Applicant | Difco Laboratories, Inc., Detroit MI, US |
| Decision | Substantially Equivalent, Jun 8, 1989 |
| Received | Mar 29, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892051
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.