FDA 510(k) Applications Submitted by Shenzhen Aeon Technology Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K200414 | 02/19/2020 | Pulse Oximeter | Shenzhen Aeon Technology Co., Ltd. |
| K190869 | 04/03/2019 | Pulse Oximeter | Shenzhen Aeon Technology Co., Ltd. |
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