510(k) K222887 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Arm Blood Pressure Monitor/Automatic Wireless Smart Blood Pressure Monitor
| Applicant | Famidoc Technology Company Limited, Dongguan, CN |
| Decision | Substantially Equivalent, Apr 10, 2023 |
| Received | Sep 23, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222887
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.