510(k) K222125 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Arm Blood Pressure Monitor, models AOJ-30A, AOJ-30B, AOJ-30C, AOJ-30D, AOJ-30E, AOJ-30F and AOJ-30G
| Applicant | Shenzhen AOJ Medical Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Dec 1, 2022 |
| Received | Jul 18, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222125
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.