510(k) K920778 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
OMRON WRIST DIGITAL BLOOD PRESSURE MONITOR HEM-601
| Applicant | Omron Healthcare, Inc., Vernon Hills IL, US |
| Decision | Substantially Equivalent, Dec 24, 1992 |
| Received | Feb 20, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920778
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.