510(k) K790761 ยท HGM System, Monitoring, Perinatal
FETASONDE MODEL 2108
| Applicant | Roche Medical Electronics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 1, 1979 |
| Received | Apr 17, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790761
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.