Scion International, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K040087 | RABBIT | April 1, 2004 |
| K973698 | SCION BALLOON ELEVATOR | March 31, 1998 |
| K973652 | DUOCLIPPER TITANIUM CLIPS | March 27, 1998 |
| K963006 | SCION SAPHENOUS VEIN HARVESTING SYSTEM | September 20, 1996 |