510(k) K880572 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
OHMEDA 2350 FINAPRES(R) BLOOD PRESSURE MONITOR
| Applicant | Ohmeda Medical, Englewood CO, US |
| Decision | Substantially Equivalent, May 10, 1988 |
| Received | Feb 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880572
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.