510(k) K880618 ยท LHD Device, Fertility Diagnostic, Proceptive
FERTILITY FORECASTER COMPUTER PROGRAM
| Applicant | Fertile Time, Ltd., Dix Hills NY, US |
| Decision | Substantially Equivalent, Jun 24, 1988 |
| Received | Feb 16, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880618
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.