510(k) K050413 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600
| Applicant | Amplife Corporation, Great Neck NY, US |
| Decision | Substantially Equivalent, Mar 4, 2005 |
| Received | Feb 18, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050413
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.