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 Churchill Corp. with 35 510(k) clearances. The most recent is a 510(k) clearance dated Apr 14, 1988: ENTERAL BAG/SET.
| Apr 14, 1988 | ENTERAL BAG/SETK880051 · KNT | 510(k) clearances |
| Apr 14, 1988 | CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETSK880026 · FPB | 510(k) clearances |
| Apr 14, 1988 | CHURCHILL 0.22 MICRON LIQUID FILTER SETSK880025 · FPB | 510(k) clearances |
| Apr 13, 1988 | CHURCHILL 1.2 MICRON LIQUID FILTER SETK880027 · FPB | 510(k) clearances |
| Oct 15, 1987 | CHURCHILL PARENTERAL NUTRITION BAG - EVAK870395 · KPE | 510(k) clearances |
| Oct 15, 1987 | CHURCHILL-CATHK872585 · FOZ | 510(k) clearances |
| Oct 13, 1987 | CHURCHILL ALBUMIN IV ADMINISTRATION SETK872124 · FPA | 510(k) clearances |
| Oct 9, 1987 | CHURCHILL TPN ADMINISTRATION SETK872123 · 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
