510(k) K960319 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
A & D UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR
| Applicant | A&D Engineering, Inc., Milpitas CA, US |
| Decision | Substantially Equivalent, Jul 2, 1996 |
| Received | Jan 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960319
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.