510(k) K902190 ยท HEK Monitor, Heart Sound, Fetal, Ultrasonic
FETAL PULSE DETECTOR MODEL DOP-1
| Applicant | Advanced Medical Systems, Inc., Hamden CT, US |
| Decision | Substantially Equivalent, Oct 22, 1990 |
| Received | May 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902190
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.