510(k) K171668 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Bluetooth blood pressure monitor
| Applicant | Visiomed Group SA, Paris, FR |
| Decision | Substantially Equivalent, Feb 26, 2018 |
| Received | Jun 5, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171668
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.