Haemoband Surgical, Ltd.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2025-10-09
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250645 | SleeveLUX 24 Anoscope/Proctoscope (P2001); SleeveLUX 16 Anoscope/Proctoscope (P2002) | FER | 2025-10-09 | View |
No matching devices.