510(k) K200163 ยท LHD Device, Fertility Diagnostic, Proceptive
Ava Fertility Tracker
| Applicant | Ava AG, Zurich, CH |
| Decision | Substantially Equivalent, Jan 19, 2021 |
| Received | Jan 22, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200163
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.