510(k) K760919 ยท HGM System, Monitoring, Perinatal
MODEL 2106 FETA SONDE FETAL MONITOR
| Applicant | Roche Medical Electronics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 16, 1976 |
| Received | Oct 28, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760919
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.