510(k) K801791 ยท FLK Thermometer, Clinical Mercury
FERTILITY AWARENESS METHOD KIT
| Applicant | Telesis Corp., Walker MI, US |
| Decision | Substantially Equivalent, Oct 31, 1980 |
| Received | Jul 29, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801791
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.