510(k) K904211 ยท LHD Device, Fertility Diagnostic, Proceptive
BIOSELF 2000 FERTILITY INDICATOR
| Applicant | Bioself, Inc., Thonex-Geneve-Suisse, CH |
| Decision | Substantially Equivalent, Oct 14, 1992 |
| Received | Sep 12, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904211
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.