510(k) K073390 ยท LFX Enzyme Linked Immunoabsorbent Assay, Rubella
DIASORIN LIASON RUBELLA IGG ASSAY; DIASORIN LIAISON RUBELLA IGG TRI-CONTROLS
| Applicant | DiaSorin, Inc., Stillwater MN, US |
| Decision | Substantially Equivalent, Nov 21, 2008 |
| Received | Dec 3, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073390
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.