510(k) K213430 ยท DQA Oximeter
Fingertip Pulse Oximeter
| Applicant | Shenzhen Witleaf Medical Electronics Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Dec 30, 2022 |
| Received | Oct 21, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213430
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.