510(k) K220886 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Upper Arm Type Blood Pressure Monitor
| Applicant | Shenzhen Jamr Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Jul 27, 2022 |
| Received | Mar 28, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220886
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.