510(k) K845009 ยท LHD Device, Fertility Diagnostic, Proceptive
RABBIT-PERSONAL COMPUTER FOR WOMEN
| Applicant | Sanimor, Inc., Beverly Hills CA, US |
| Decision | Substantially Equivalent, Apr 10, 1985 |
| Received | Dec 26, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K845009
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.