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 Dilab, Inc. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Apr 21, 1987: RAPID AS LATEX.
| Date | Record | Source |
|---|---|---|
| Apr 21, 1987 | RAPID AS LATEXK862530 · GTQ | 510(k) clearances |
| Jun 26, 1985 | ALBUMINK850931 · CIX | 510(k) clearances |
| Jun 25, 1985 | TOTAL PROTEINSK850936 · CEK | 510(k) clearances |
| Jun 25, 1985 | PHOSPHORUSK850934 · CEO | 510(k) clearances |
| Jun 25, 1985 | CREATININEK850932 · CGX | 510(k) clearances |
| Jun 25, 1985 | CHOLESTEROLK850938 · CGO | 510(k) clearances |
| Jun 25, 1985 | URIC ACIDK850933 · CDH | 510(k) clearances |
| Jun 10, 1985 | GLUCOSEK850930 · CGE | 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
