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 Vistek Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 18, 1990: VISTEK ELECTRONIC CONTROLLER.
| Dec 18, 1990 | VISTEK ELECTRONIC CONTROLLERK904682 · GEY | 510(k) clearances |
| Dec 18, 1990 | VLS 5300 300W XENON LIGHT SOURCEK904681 · HBI | 510(k) clearances |
| Apr 10, 1987 | LCA 2000K871034 · FTA | 510(k) clearances |
| Feb 7, 1986 | VIS-2000 VIDEO SYSTEMK860173 · FWG | 510(k) clearances |
| Dec 12, 1984 | VIS-1000 VIDEO SYSTEMK843806 · KQM | 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
