510(k) K030561 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODELS HPL-100 AND HPL-100A
| Applicant | Mytech Technology Co., Ltd., Columbus OH, US |
| Decision | Substantially Equivalent, May 9, 2003 |
| Received | Feb 21, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030561
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.