510(k) K071523 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR, MODELS BP1600, BP1650, BP1700 AND BP1750
| Applicant | Genexel-Sein, Inc., Roswell GA, US |
| Decision | Substantially Equivalent, Jun 26, 2007 |
| Received | Jun 4, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071523
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.