# Leeco Diagnostics, Inc.

- Location (FDA's records): Southfield, MI
- FDA decisions: 49 (1979–1989): 49 510(k) clearances
- Product codes: JHI (10), CDZ (4), CEP (4), GTZ (3), CFT (3), CGJ (2), JFH (2), CDP (2), JLW (2), LCX (2), DHA (2), LCP (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K895765: Leeco Preview (R) Ebv (Eia) (Oct 31, 1989)
- K894122: Leeco Vis-Disk Strep-a (Eia) (Aug 15, 1989)
- K891095: Vis-Disk HCG (Eia) Lyophilized JPL-044M (Jun 16, 1989)
- K891096: Vis-Disk HCG (Eia) JPL-041M (Jun 16, 1989)
- K883269: PRL-Quant (Sep 13, 1988)
- K880577: Concep-7-BHCG (Mar 15, 1988)
- K880069: Leeco Pregnastick (Eia) Catalog #003 (Feb 11, 1988)
- K870259: Vis-Cube HCG (Eia) Lyophilized JPL-044 (Mar 10, 1987)

Source page: https://510kreport.com/company/leeco-diagnostics