510(k) K061959 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
MYTECH / HAPPY LIFE / MAXIAIDS ARM BLOOD PRESSURE MONITOR, HPL-301, HPL-302, HPL-310, 180310
| Applicant | Mytech Technology Co., Ltd., Hsin-Chu City, TW |
| Decision | Substantially Equivalent, Aug 22, 2006 |
| Received | Jul 11, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061959
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.