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 Becton DickinsonLabelled 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 Viasys Medsystems with 7 510(k) clearances. The most recent is a 510(k) clearance dated Nov 7, 2008: ENTERAL PUMP SET, MODEL 20-1010.
| Nov 7, 2008 | ENTERAL PUMP SET, MODEL 20-1010K081725 · KNT | 510(k) clearances |
| Jun 27, 2008 | MODIFICATION TO CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900K080679 · KNT | 510(k) clearances |
| Apr 2, 2007 | CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900K063061 · KNT | 510(k) clearances |
| May 6, 2005 | ANTI-I.V. ENTERAL FEEDING SYSTEMK043044 · KNT | 510(k) clearances |
| Mar 25, 2005 | PULMANEX DISPOSABLE PRESSURE MANOMETER, MODEL 50-5000K050309 · CAP | 510(k) clearances |
| Mar 16, 2005 | STACKHOUSE FREEDOMAIRE II SURGICAL HELMET SYSTEM, MODELS 12000, 12010, 12011, 12020, 12021, 12022, 12030, 12031K043004 · FYA | 510(k) clearances |
| Dec 17, 2004 | CORTRAKK041987 · KNT | 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
