Sightline Technologies , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K032688 | COLONOSIGHT MODEL 510B | March 5, 2004 |
| K011825 | RECTOSIGHT RS300-04;AND PROTOSIGHT PS300-04 DEVICE | July 11, 2001 |
| K994130 | RECTOSIGHT RS 300-04 | June 30, 2000 |