GEMSS HEALTHCARE CO., LTD.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest Approval2023-11-16
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K233200 | XPLUS 35 Series (XPLUS 35, XPLUS 35FD) | OWB | 2023-11-16 | View |
| 510(k) | K230800 | XVISION-525, HORIZON, HI-300, HI-500, SATURN-F PF32, SATURN-F PF40, SATURN-F PF50 | KPR | 2023-11-02 | View |
No matching devices.