510(k) K221212 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Upper Arm Blood Pressure Monitor
| Applicant | Shenzhen Yolanda Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Aug 26, 2022 |
| Received | Apr 27, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221212
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.