Vascular Architects, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K031641 | VASCULAR ARCHITECTS ASPIRE COVERED STENT AND 718 DELIVERY SYSTEM | August 1, 2003 |
| K030567 | MODIFICATION TO VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTRILLED EXPANSION DELIVERY SYSTEM | March 24, 2003 |
| K012544 | VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTROLLED EXPANSION DELIVERY SYSTEM | November 15, 2001 |
| K003173 | ASPIRE COVERED STENT AND DELIVERY CATHETER | March 13, 2001 |
| K003719 | VASCULAR ARCHITECTS PERISCOPE DEVICE | February 28, 2001 |