510(k) K090510 ยท KNG Monitor, Ultrasonic, Fetal
DOPPLER FETAL HEARTBEAT RATE DETECTOR
| Applicant | Shenzhen Bestman Instrument Co., Ltd., Guangdong, CN |
| Decision | Substantially Equivalent, Apr 29, 2010 |
| Received | Feb 26, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090510
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.