510(k) K832171 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
SELF CHECK DIGITAL BLOOD PRESS. MONITOR
| Applicant | Ritter Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 4, 1983 |
| Received | Jul 6, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832171
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.