510(k) K791038 ยท HGM System, Monitoring, Perinatal
FETASONDE UTERINE ACTIVITY MONITOR
| Applicant | Roche Medical Electronics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 4, 1979 |
| Received | Jun 5, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791038
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.