510(k) K781906 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
BLOOD PRESSURE DEVICE, 400 SERIES
| Applicant | Med-Tek Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 16, 1978 |
| Received | Nov 13, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781906
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.