510(k) K981729 ยท LFX Enzyme Linked Immunoabsorbent Assay, Rubella
IS-RUBELLA IGG TEST SYSTEM
| Applicant | Diamedix Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jan 28, 1999 |
| Received | May 15, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981729
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.