Arterial Vascular Engineering, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K984627 | AVE 4F SITESEER CARDIOVASCULAR ANGIOGRAPHIC CATHETER | July 27, 1999 |
| K983927 | GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORT | March 11, 1999 |
| K971295 | AVE BRIDGE STENT SYSTEM | November 5, 1997 |