510(k) K890091 ยท LFX Enzyme Linked Immunoabsorbent Assay, Rubella
MODIFIED LABSYSTEMS' RUBELLA IGG EIA TEST KIT
| Applicant | Labsystems, Inc., Finland, FI |
| Decision | Substantially Equivalent, Feb 3, 1989 |
| Received | Jan 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890091
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.