510(k) K220106 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
QardioArm 2
| Applicant | Qardio, Inc., San Fransciso CA, US |
| Decision | Substantially Equivalent, Jun 15, 2022 |
| Received | Jan 12, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220106
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.