510(k) K232989 ยท DQA Oximeter
Pulse Oximeter (AOJ-70A); Pulse Oximeter (AOJ-70B); Pulse Oximeter (AOJ-70C); Pulse Oximeter (AOJ-70D); Pulse Oximeter (AOJ-70E)
| Applicant | Shenzhen AOJ Medical Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Jul 1, 2024 |
| Received | Sep 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232989
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.