510(k) K810662 ยท CEP Radioimmunoassay, Luteinizing Hormone
LEECO LH-QUANT DIAGNOSTIC KIT
| Applicant | Leeco Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 31, 1981 |
| Received | Mar 11, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810662
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.