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 Applied Vascular Devices with 21 510(k) clearances. The most recent is a 510(k) clearance dated Dec 23, 1991: SURGICAL OBTURATOR WITH SEAL.
| Dec 23, 1991 | SURGICAL OBTURATOR WITH SEALK911730 · GCJ | 510(k) clearances |
| Jul 5, 1991 | DISPOSABLE SURGICAL TROCAR WITH SEALK911589 · GCJ | 510(k) clearances |
| May 29, 1991 | AVD INTIMAX OCCLUSION CATHETERK910339 · DQT | 510(k) clearances |
| Apr 26, 1991 | INTIMAX THROMBECTOMY CATHETERK910372 · DXE | 510(k) clearances |
| Apr 18, 1991 | INTIMAX(TM) IRRIGATION CATHETERK911181 · GCA | 510(k) clearances |
| Mar 28, 1991 | AVD INTIMAX CHOLANGIOGRAPHY CATHETERK910493 · FGE | 510(k) clearances |
| Mar 25, 1991 | DIAGNOSTIC INTRASCULAR CATHETERK903848 · DQO | 510(k) clearances |
| Mar 21, 1991 | OPERATIVE CHOLANGIOGRAPHIC CATHETERK905738 · FGE | 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
