Diagnostics 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 Crestat Diagnostics with 29 510(k) clearances. The most recent is a 510(k) clearance dated Sep 3, 1998: N-ASSAY GLU-UL.
| Date | Record | Source |
|---|---|---|
| Sep 3, 1998 | N-ASSAY GLU-ULK980883 · CFR | 510(k) clearances |
| May 1, 1998 | N-ASSAY L D-BILK981276 · CIG | 510(k) clearances |
| Apr 27, 1998 | N-ASSAY L T-BILK981289 · CIG | 510(k) clearances |
| Mar 26, 1998 | N-ASSAY CPK-LK980900 · CGS | 510(k) clearances |
| Mar 26, 1998 | N-ASSAY L AST/GOTK980902 · CIT | 510(k) clearances |
| Oct 20, 1997 | N-ASSAY TIA PLASMINOGEN TEST KITK971985 · GGP | 510(k) clearances |
| Oct 20, 1997 | N-ASSAY TIA ANTITHROMBIN III TEST KITK972257 · DDQ | 510(k) clearances |
| Aug 1, 1997 | N-ASSAY TIA APO B TEST KITK964296 · DER | 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
