510(k) K911871 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
CARDIODYNE KINETORR/PC BLOOD PRESSURE MONITORS
| Applicant | Cardiodyne, Inc., Brookline MA, US |
| Decision | Substantially Equivalent, Nov 7, 1991 |
| Received | Apr 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911871
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.