510(k) K220113 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Upper Arm Electronic Blood Pressure Monitor(Model FC-BP100,FC-BP101,FC-BP102,FC-BP110,FC-BP111,FC-BP112)
| Applicant | Shenzhen Finicare Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, May 31, 2022 |
| Received | Jan 14, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220113
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.