510(k) K780487 ยท HFO Recorder, Pressure, Intrauterine
FETAL MONITORING SYSTEM
| Applicant | Sonicaid, Inc. VA, US |
| Decision | Substantially Equivalent, May 9, 1978 |
| Received | Mar 27, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780487
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.