510(k) K896642 ยท CEP Radioimmunoassay, Luteinizing Hormone
MODIFIED LH ENZYME IMMUNOASSAY TEST KIT
| Applicant | Medix Biotech, Inc., Foster City CA, US |
| Decision | Substantially Equivalent, Jan 30, 1990 |
| Received | Nov 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896642
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.