510(k) K850579 ยท NGE Test, Luteinizing Hormone (Lh), Over The Counter
CUE FERTILITY MONITOR
| Applicant | Zetek, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Mar 22, 1985 |
| Received | Feb 13, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850579
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.