510(k) K231367 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Wrist Electronic Blood Pressure Monitor(Model FC-BP200, FC-BP201, FC-BP210,FC-BP211, FC-BP220, FC-BP221)
| Applicant | Shenzhen Finicare Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Sep 18, 2023 |
| Received | May 11, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231367
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.