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 Elite Technology, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 10, 1990: PROTEIN TEST FOR URINE AND CSF.
| Date | Record | Source |
|---|---|---|
| Jul 10, 1990 | PROTEIN TEST FOR URINE AND CSFK900733 · CEK | 510(k) clearances |
| May 23, 1990 | URIC ACID TEST KITK901001 · KNK | 510(k) clearances |
| Mar 29, 1990 | ELITECH GAMMA GT TEST KITK901090 · JPZ | 510(k) clearances |
| Feb 16, 1990 | CHOLESTEROL TEST KITK895951 · CHH | 510(k) clearances |
| Jan 11, 1990 | TRIGLYCERIDES TEST KITK895952 · CDT | 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
