510(k) K242002 ยท LKF Cannula, Manipulator/Injector, Uterine
FemVue MINI Saline-Air Device
| Applicant | Femasys, Inc., Suwanee GA, US |
| Decision | Substantially Equivalent, Nov 22, 2024 |
| Received | Jul 9, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242002
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.