510(k) K881771 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
SENSOCOR(TM) DIASYS
| Applicant | Sensormedix, Inc., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Jan 12, 1989 |
| Received | Apr 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881771
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.