Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Pausch Corp. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Dec 5, 2008: HDR VISION, VISION HDR, HD R/F, UROMAT HD R/F.
| Date | Record | Source |
|---|---|---|
| Dec 5, 2008 | HDR VISION, VISION HDR, HD R/F, UROMAT HD R/FK081073 · OWB | 510(k) clearances |
| Jun 17, 1998 | COMBI ELEVATOR-2 & COMBI ELEVATOR-2 TOMOK973864 · IZF | 510(k) clearances |
| Apr 30, 1998 | CS2000 & CS2000 TOMOK973834 · IZF | 510(k) clearances |
| Aug 30, 1990 | UROMAT 2000K903395 · IXR | 510(k) clearances |
| Mar 30, 1987 | COSMOSK870856 · IYB | 510(k) clearances |
| Apr 26, 1979 | KS-78 VERTICAL WALL CASSETTE HOLDERK790742 · IXY | 510(k) clearances |
| Apr 26, 1979 | BS 66, UNIVERSAL BUCKY STANDK790740 · KPR | 510(k) clearances |
| Apr 26, 1979 | COMPACT SYSTEMK790741 · KPR | 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
