510(k) K030221 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR
| Applicant | Mytech Technology Co., Ltd., Hsin-Chu City, TW |
| Decision | Substantially Equivalent, Jul 25, 2003 |
| Received | Jan 21, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030221
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.