Sightline Technologies , 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) | K032688 | COLONOSIGHT MODEL 510B | FDF | 2004-03-05 | View |
| 510(k) | K011825 | RECTOSIGHT RS300-04;AND PROTOSIGHT PS300-04 DEVICE | FER | 2001-07-11 | View |
| 510(k) | K994130 | RECTOSIGHT RS 300-04 | FER | 2000-06-30 | View |
No matching devices.
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