510(k) K904600 ยท MAA Monitor, Fetal Doppler Ultrasound
L582 TRANSDUCER
| Applicant | Acuson Corp., Mountain View CA, US |
| Decision | Substantially Equivalent, Jun 24, 1991 |
| Received | Oct 10, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904600
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.