510(k) K030230 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
AVITA BPM1 SERIES (WRIST TYPE) BLOOD PRESSURE METER (OR MONITOR)
| Applicant | Avita Corporation, Flagstaff AZ, US |
| Decision | Substantially Equivalent, May 23, 2003 |
| Received | Jan 22, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030230
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.