510(k) K873764 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
AMBULATORY BLOOD PRESSURE MONITOR
| Applicant | Pulsetrend, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 10, 1988 |
| Received | Sep 16, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873764
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.