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 Leeco Diagnostics with 49 510(k) clearances. The most recent is a 510(k) clearance dated Oct 31, 1989: LEECO PREVIEW(R) EBV (EIA).
| Date | Record | Source |
|---|---|---|
| Oct 31, 1989 | LEECO PREVIEW(R) EBV (EIA)K895765 · KTN | 510(k) clearances |
| Aug 15, 1989 | LEECO VIS-DISK STREP-A (EIA)K894122 · GTZ | 510(k) clearances |
| Jun 16, 1989 | VIS-DISK HCG (EIA) JPL-041MK891096 · DHA | 510(k) clearances |
| Jun 16, 1989 | VIS-DISK HCG (EIA) LYOPHILIZED JPL-044MK891095 · DHA | 510(k) clearances |
| Sep 13, 1988 | PRL-QUANTK883269 · CFT | 510(k) clearances |
| Mar 15, 1988 | CONCEP-7-BHCGK880577 · JHI | 510(k) clearances |
| Feb 11, 1988 | LEECO PREGNASTICK (EIA) CATALOG #003K880069 · LCX | 510(k) clearances |
| Mar 10, 1987 | VIS-CUBE HCG (EIA) LYOPHILIZED JPL-044K870259 · JHI | 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
