510(k) K821507 ยท LHD Device, Fertility Diagnostic, Proceptive
SYMPTOTHERM 8 FERTILITY INDICATOR
| Applicant | Ovix Corp., Inc., Walker MI, US |
| Decision | Substantially Equivalent, Oct 14, 1982 |
| Received | May 20, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821507
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.