510(k) K212900 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
MX7/MX7T/Vaus7/Zeus/ME7/Anesus ME7/Anesus ME7T/MX8/MX8T/Vaus8/ME8 Diagnostic Ultrasound System
| Applicant | Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Nov 5, 2021 |
| Received | Sep 13, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212900
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.