510(k) K110288 ยท LKF Cannula, Manipulator/Injector, Uterine
FEMVUE SALINE-AIR DEVICE
| Applicant | Femasys, Inc., Suwanee GA, US |
| Decision | Substantially Equivalent, Apr 28, 2011 |
| Received | Feb 1, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110288
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.