510(k) K213431 ยท DQA Oximeter
Handheld Pulse Oximeter
| Applicant | Shenzhen Witleaf Medical Electronics Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Feb 26, 2023 |
| Received | Oct 21, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213431
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.