510(k) K072976 ยท HGM System, Monitoring, Perinatal
MODEL 250CX SERIES MATERNAL/FETAL MONITOR
| Applicant | GE Healthcare, Laurel MD, US |
| Decision | Substantially Equivalent, Dec 20, 2007 |
| Received | Oct 25, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072976
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.