510(k) K242846 ยท KNG Monitor, Ultrasonic, Fetal
Doppler FHR Detector (BF-500D+, BF-560)
| Applicant | Shenzhen Bestman Instrument Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Jun 26, 2025 |
| Received | Sep 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242846
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.