510(k) K231730 ยท MQF Catheter, Assisted Reproduction
FemaSeed Intratubal Insemination
| Applicant | Femasys, Inc., Suwanee GA, US |
| Decision | Substantially Equivalent, Sep 22, 2023 |
| Received | Jun 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231730
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.