510(k) K900618 ยท KNG Monitor, Ultrasonic, Fetal
HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140
| Applicant | Huntleigh Technology, Inc., Manalapan NJ, US |
| Decision | Substantially Equivalent, Apr 25, 1990 |
| Received | Feb 8, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900618
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.