510(k) K904739 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
DYNAPULSE 200M
| Applicant | Pulse Metric, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jan 8, 1991 |
| Received | Oct 18, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904739
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.