510(k) K901392 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
BP50 BLOOD PRESSURE AND PULSE MONITOR
| Applicant | Pulse Time Products, Ltd., Chichester, W. Sussex, GB |
| Decision | Substantially Equivalent, Aug 23, 1990 |
| Received | Mar 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901392
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.