510(k) K230172 ยท DQA Oximeter
Pulse Oximeter
| Applicant | Beijing Choice Electronic Technology Co., Ltd., Beijing, CN |
| Decision | Substantially Equivalent, Aug 12, 2023 |
| Received | Jan 20, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230172
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.