Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Advanced Vascular Dynamics with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jul 31, 2015: Zephyr Vascular Compression Device.
| Jul 31, 2015 | Zephyr Vascular Compression DeviceK151363 · DXC | 510(k) clearances |
| Dec 4, 2014 | RADAR VASCULAR COMPRESSION DEVICEK142122 · DXC | 510(k) clearances |
| Jan 31, 2014 | AVD RIGHT RADIAL DRAPEK131571 · KKX | 510(k) clearances |
| Feb 12, 2010 | FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICEK093192 · JOM | 510(k) clearances |
| Nov 19, 2009 | RADAR VASCULAR COMPRESSION DEVICESK092503 · DXC | 510(k) clearances |
| Mar 23, 2009 | PRESSUREMATE MANUAL FEMORAL ACCESS COMPRESSION DEVICEK090286 · DXC | 510(k) clearances |
| Sep 6, 2007 | COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICEK072167 · DXC | 510(k) clearances |
| Jun 1, 2004 | COMPRESSAR SUPERCOMFORT DISC AND STRONGARM SUPERCOMFORT SYSTEMK040615 · DXC | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
