510(k) K091739 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
SEMI AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODELS KD-3917, KD 3909
| Applicant | Andon Health Co, Ltd., Tianjin, CN |
| Decision | Substantially Equivalent, Aug 18, 2009 |
| Received | Jun 11, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091739
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.