510(k) K222798 ยท LKF Cannula, Manipulator/Injector, Uterine
Rejoni Intrauterine Catheter
| Applicant | Rejoni, Inc., Bedford MA, US |
| Decision | Substantially Equivalent, Dec 16, 2022 |
| Received | Sep 16, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222798
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.