510(k) K830035 ยท LFM Enzyme Immunoassay, Digitoxin
SOPHEIA DIGITOXIN EIA KIT & COMPONENTS
| Applicant | Diagnostic Products Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 28, 1983 |
| Received | Jan 7, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830035
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.