510(k) K882635 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
ELECTRONIC DIGITAL BLOOD PRESSURE MONITOR
| Applicant | Nihon Seimitsu Sokki Co., Ltd., Shibukawa-Shi, Gunma-Ken, JP |
| Decision | Substantially Equivalent, Nov 9, 1988 |
| Received | Jun 27, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882635
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.