510(k) K222327 ยท HGM System, Monitoring, Perinatal
Bloomlife MFM-Pro
| Applicant | Bloom Technologies NV, Genk, BE |
| Decision | Substantially Equivalent, Feb 13, 2023 |
| Received | Aug 2, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222327
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.