Advanced Vascular Dynamics
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K151363 | Zephyr Vascular Compression Device | July 31, 2015 |
| K142122 | RADAR VASCULAR COMPRESSION DEVICE | December 4, 2014 |
| K131571 | AVD RIGHT RADIAL DRAPE | January 31, 2014 |
| K093192 | FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE | February 12, 2010 |
| K092503 | RADAR VASCULAR COMPRESSION DEVICES | November 19, 2009 |
| K090286 | PRESSUREMATE MANUAL FEMORAL ACCESS COMPRESSION DEVICE | March 23, 2009 |
| K072167 | COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE | September 6, 2007 |
| K040615 | COMPRESSAR SUPERCOMFORT DISC AND STRONGARM SUPERCOMFORT SYSTEM | June 1, 2004 |