510(k) K991739 ยท HGM System, Monitoring, Perinatal
COROMETRICS 120 SERIES MATERNAL/FETAL MONITOR
| Applicant | General Electric Medical Systems Information Techn, Annapolis MD, US |
| Decision | Substantially Equivalent, Aug 19, 1999 |
| Received | May 21, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991739
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.