510(k) K915138 ยท MAA Monitor, Fetal Doppler Ultrasound
GE SONOCHROME
| Applicant | GE Medical Systems, Waukesha WI, US |
| Decision | Substantially Equivalent, Oct 20, 1992 |
| Received | Nov 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915138
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.