# Livonia Diagnostics, Inc.

- Location (FDA's records): Livonia, MI
- FDA decisions: 16 (1984–1985): 16 510(k) clearances
- Product codes: CIC (1), CEO (1), CHH (1), CKD (1), CDW (1), CIO (1), CGA (1), JGJ (1), GHM (1), CEK (1), LBR (1), CGX (1)
- 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
- K852161: Serum Iron/Vibc Reagent Set (Jun 10, 1985)
- K844283: SGPT Reagent Set (Nov 27, 1984)
- K844322: Sgot Reagent Set (Nov 27, 1984)
- K844237: Alkaline Phosphatase Reagent Set (Nov 20, 1984)
- K844156: Urea Nitrogen Reagent Set (Nov 13, 1984)
- K844182: Inorganic Phosphorus Reagent Set (Nov 9, 1984)
- K843894: HDL Precipatating Reagent Set (Nov 2, 1984)
- K843895: Total Calcium Reagent Set (Oct 30, 1984)

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