510(k) K182190 ยท KNG Monitor, Ultrasonic, Fetal
Fetal Doppler
| Applicant | Shenzhen AOJ Medical Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Dec 19, 2018 |
| Received | Aug 13, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182190
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.