Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of AbbottLabelled by claude-sonnet-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 15, 2026, FDA's public records list Devices for Vascular Intervention, Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Mar 10, 1994: MICROTRACK.
| Mar 10, 1994 | MICROTRACKK935929 · MCW | 510(k) clearances |
| Nov 23, 1992 | HOLLOW MOTOR DRIVE UNIT W/ TORQUE CONTROLLERK920707 · MCW | 510(k) clearances |
| Dec 18, 1991 | DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVEK914422 · DQY | 510(k) clearances |
| Jul 12, 1991 | ROTATING HEMOSTATIC VALVEK911678 · DYB | 510(k) clearances |
| Feb 25, 1991 | LP-60 LOW PRESSURE INFLATION DEVICEK910205 · MAV | 510(k) clearances |
| Jul 6, 1990 | HOLLOW MOTOR DRIVE UNITK901601 · LIT | 510(k) clearances |
| Dec 2, 1988 | INTRODUCING CATHETERK883933 · DYB | 510(k) clearances |
| Nov 3, 1988 | GUIDING CATHETER (TIP SOFTNESS CHANGE)K883981 · DWF | 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
