510(k) K172880 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Microlife Upper Arm Automatic Digital Blood Pressure Monitor
| Applicant | Microlife Intellectual Property GmbH, Widnau, CH |
| Decision | Substantially Equivalent, Apr 18, 2018 |
| Received | Sep 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172880
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.