510(k) K854838 ยท CEP Radioimmunoassay, Luteinizing Hormone
LEE-BEAD BETA LH (EIA)
| Applicant | Leeco Diagnostics, Inc., Southfield MI, US |
| Decision | Substantially Equivalent, Jan 7, 1986 |
| Received | Dec 3, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854838
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.