510(k) K901512 ยท LHD Device, Fertility Diagnostic, Proceptive
L SOPHIA
| Applicant | Nishitomo Co., Inc., Japan, JP |
| Decision | Substantially Equivalent, Jul 20, 1990 |
| Received | Mar 29, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901512
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.