510(k) K890139 ยท KNG Monitor, Ultrasonic, Fetal
TOITU DOPPLER FETUS DETECTOR, FD-400D
| Applicant | Toitu of America, Inc., Wayne PA, US |
| Decision | Substantially Equivalent, Mar 29, 1989 |
| Received | Jan 13, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890139
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.