510(k) K231303 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Arm-type Fully Automatic Digital Blood Pressure Monitor
| Applicant | Joytech Healthcare Co. , Ltd., Hangzhou, CN |
| Decision | Substantially Equivalent, Jan 26, 2024 |
| Received | May 5, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231303
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.