510(k) K963613 ยท LFX Enzyme Linked Immunoabsorbent Assay, Rubella
IMMULITE RUBELLA IGG
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Apr 2, 1997 |
| Received | Sep 10, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963613
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.