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.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Viatronix with 8 510(k) clearances. The most recent is a 510(k) clearance dated Dec 5, 2008: VIATRONIX V3D-CARDIAC, REVISION 1.0.
| Dec 5, 2008 | VIATRONIX V3D-CARDIAC, REVISION 1.0K083293 · JAK | 510(k) clearances |
| Apr 19, 2004 | VIATRONIX V3D COLON, REVISION 1.3K040126 · LLZ | 510(k) clearances |
| Nov 5, 2003 | VIATRONIX V3D VASCULAR, REVISION 1.0K033361 · LLZ | 510(k) clearances |
| Aug 22, 2003 | VIATRONIX V3D EXPLORER, REVISION 1.2K032483 · LLZ | 510(k) clearances |
| Sep 6, 2002 | VIATRONIX V3D EXPLORERK022789 · LLZ | 510(k) clearances |
| Mar 7, 2002 | VIATRONIX V3D COLONK020658 · LLZ | 510(k) clearances |
| Dec 7, 2001 | VIATRONIC V3D CALCIUM SCORINGK013146 · JAK | 510(k) clearances |
| Nov 17, 2000 | VIATRONIX VISUALIZATION SYSTEM (VVS)K002780 · LLZ | 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
