510(k) K790951 ยท KNG Monitor, Ultrasonic, Fetal
SA/7860 FETAL HEART MONITOR (DOPPLER)
| Applicant | Schlosser Alberti Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 3, 1979 |
| Received | May 21, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790951
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.