510(k) K014204 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822
| Applicant | K-Jump Health Co., Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Mar 5, 2002 |
| Received | Dec 21, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014204
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.