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 13, 2026, FDA's public records list Venospital with 14 510(k) clearances. The most recent is a 510(k) clearance dated Sep 4, 1979: FLU VEN TR-1.
| Sep 4, 1979 | FLU VEN TR-1K791131 · KSB | 510(k) clearances |
| Sep 4, 1979 | FLU-VEN TK-2K791130 · KSB | 510(k) clearances |
| Apr 30, 1979 | FLU-VEN 01510K790424 · FPA | 510(k) clearances |
| Apr 30, 1979 | BIOSTIL # 3884K790077 · FPA | 510(k) clearances |
| Aug 10, 1978 | INFUSION SET W/ INJECTION SITE, 23D-WK781187 · FPA | 510(k) clearances |
| Aug 10, 1978 | INFUSION SET, VENOTHIN 25K781188 · FPA | 510(k) clearances |
| Aug 10, 1978 | INFUSION, VENOTHIN 23K781186 · FPA | 510(k) clearances |
| Aug 10, 1978 | FLU VEN 0151K781189 · FPA | 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
