Haemoband Surgical, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| 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 |
| 510(k) | K091519 | HAEMOBAND MULTI-LIGATOR | FHN | 2009-07-28 | View |
No matching devices.
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