Shenzhen Aeon Technology Co., Ltd.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K200414 | Pulse Oximeter | DQA | 2020-09-23 | View |
| 510(k) | K190869 | Pulse Oximeter | DQA | 2019-09-13 | View |
| 510(k) | K171578 | Infrared thermometer | FLL | 2017-11-30 | View |
No matching devices.
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