Nantong Egens Biotechnology Co., Ltd.
FDA 510(k) & PMA Approved Devices — 1 products
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Total Devices1
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232864 | EGENS Pregnancy Test Midstream I, EGENS Pregnancy Test Midstream II | LCX | 2024-01-26 | View |
No matching devices.
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