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 15, 2026, FDA's public records list Viggo Products with 7 510(k) clearances. The most recent is a 510(k) clearance dated May 29, 1985: VIGGO ACCESSORIES FOR I.V. THERAPY.
| May 29, 1985 | VIGGO ACCESSORIES FOR I.V. THERAPYK850769 · FPA | 510(k) clearances |
| Apr 12, 1985 | VIGGO NEOFLON INFUSION CANNULAK850276 · FOZ | 510(k) clearances |
| Apr 12, 1985 | VIGGO I.V. ACCESSORIES-VIGGO EXTENSION TUBES ETC.K850277 · FPA | 510(k) clearances |
| Apr 11, 1985 | VIGGO CONNECTA 3-WAY INFUSION STOPCOCKK850280 · FMG | 510(k) clearances |
| Apr 11, 1985 | VIGGO SECALON T CATHETERK850460 · FOZ | 510(k) clearances |
| Apr 9, 1985 | VASCULON I.V. CANNULAEK850278 · FOZ | 510(k) clearances |
| Apr 9, 1985 | VIGGO ARTERIAL CANNULAK850349 · FOZ | 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
