510(k) K964235 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL
| Applicant | Industrielle Entwicklung Medizintechnik Und Vertri, Stamford CT, US |
| Decision | Substantially Equivalent, Mar 2, 1999 |
| Received | Oct 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964235
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.