510(k) K171379 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Digital Automatic Wrist Blood Pressure Monitor MD4300
| Applicant | Grandway Technology (Shenzhen) Limited, Shenzhen, CN |
| Decision | Substantially Equivalent, Apr 10, 2018 |
| Received | May 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171379
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.