510(k) K780046 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
ULTRASPHYG BLOOD PRESSURE OPTION
| Applicant | Cavitron Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 15, 1978 |
| Received | Jan 9, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780046
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.