510(k) K102624 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
AVITA WRIST TYPE BLOOD PRESSURE MONITOR
| Applicant | Avita Corporation, Flagstaff AZ, US |
| Decision | Substantially Equivalent, Dec 16, 2010 |
| Received | Sep 13, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102624
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.