510(k) K250765 ยท DXQ Blood Pressure Cuff
AViTA Arm Type Blood Pressure Monitor Cuff
| Applicant | Avita Corporation, New Taipei City, TW |
| Decision | Substantially Equivalent, Sep 3, 2025 |
| Received | Mar 13, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250765
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.