510(k) K202785 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
Resona R9,Resona R9 Exp,Resona R9 Pro,Resona R9S, Nuewa R9,Nuewa R9 Exp,Nuewa R9 Pro,Nuewa R9S,Resona 7,Resona 7CV,Resona 7EXP,Resona 7S, Resona 7OB,Resona 7PRO,Imagyn 7,Resona Y Diagnostic Ultrasound System
| Applicant | Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Apr 8, 2021 |
| Received | Sep 22, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202785
No recall in the FDA data names this 510(k).
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