510(k) K221046 ยท LQK Home Uterine Activity Monitor
Invu by Nuvo
| Applicant | Nuvo- Group , Ltd., Tel Aviv, IL |
| Decision | Substantially Equivalent, May 6, 2022 |
| Received | Apr 8, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K221046
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.