510(k) K914260 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
4240 DYNAMIC BP/HEART RATE MONITOR
| Applicant | Suntech Medical Instruments, Inc., Raleigh NC, US |
| Decision | Substantially Equivalent, Sep 4, 1992 |
| Received | Sep 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914260
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.