510(k) K191673 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Upper Arm Blood Pressure Monitor
| Applicant | Famidoc Technology Company Limited, Dongguan, CN |
| Decision | Substantially Equivalent, Nov 27, 2019 |
| Received | Jun 24, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191673
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.