510(k) K863121 ยท NGE Test, Luteinizing Hormone (Lh), Over The Counter
PEAK OVULATION PREDICTOR
| Applicant | Micron Technology, Inc., Boise ID, US |
| Decision | Substantially Equivalent, Oct 14, 1986 |
| Received | Aug 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863121
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.