510(k) K190869 ยท DQA Oximeter
Pulse Oximeter
| Applicant | Shenzhen Aeon Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Sep 13, 2019 |
| Received | Apr 3, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190869
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.