510(k) K923344 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
ELECTRONIC DIGITAL BLOOD PRESSURE MONITOR
| Applicant | Citizen Watch Co., Ltd., Los Angeles CA, US |
| Decision | Substantially Equivalent, Oct 7, 1993 |
| Received | Jun 18, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923344
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.