510(k) K172780 ยท KNG Monitor, Ultrasonic, Fetal
SD1 Ultrasonic Pocket Doppler
| Applicant | Edan Instruments, Inc., Shenzhen, CN |
| Decision | Substantially Equivalent, Jun 6, 2018 |
| Received | Sep 14, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172780
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.