510(k) K242721 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Upper Arm Electronic Blood Pressure Monitor (FC-BP103, FC-BP106, FC-BP113, FC-BP120, FC-BP121, FC-BP130, FC-BP131)
| Applicant | Shenzhen Finicare Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Oct 4, 2024 |
| Received | Sep 10, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K242721
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.