510(k) K210699 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
Resona I9, Resona I9 Exp, Resona I9S, Resona I9T, Resona I9 Easi, Resona I9 Nasa, Resona IV, Imagyn I9, Imagyn I9S, Imagyn I9 Easi, Nuewa I9, Nuewa I9S, Nuewa I9T, Nuewa I9 Exp, Nuewa I9 Easi, Anesus I9, Anesus I9 Easi, Eagus I9 Diagnostic Ultrasound System
| Applicant | Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Nanshan Shenzhen, CN |
| Decision | Substantially Equivalent, Jun 10, 2021 |
| Received | Mar 9, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210699
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.