510(k) K093452 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR MODEL KD-571, KD-7971
| Applicant | Andon Health Co, Ltd., Tianjin, CN |
| Decision | Substantially Equivalent, Dec 23, 2009 |
| Received | Nov 5, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093452
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.