# Omega Medical Electronics

- Location (FDA's records): Mchenry, IL
- FDA decisions: 21 (1982–1983): 21 510(k) clearances
- Product codes: CFJ (1), CHD (1), CIQ (1), GKK (1), CKA (1), CIG (1), CDT (1), CEO (1), CIT (1), CEK (1), CGE (1), CIC (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
- K823691: Phosphorus Reagent Set (Jan 7, 1983)
- K821206: SGPT-UV Reagent Set (Jul 22, 1982)
- K821212: Urea Nitrogen Reagent Set (Jul 22, 1982)
- K821204: Glucose (Enzymatic) Reagent Set (Jul 22, 1982)
- K821201: LDH-UV Reagent Set (Jul 20, 1982)
- K821205: Triglyceride Reagent Set (Jul 20, 1982)
- K821208: Sgot-UV Reagent Set (Jul 20, 1982)
- K821209: Sgot Reagent Set (Jul 14, 1982)

Source page: https://510kreport.com/company/omega-medical-electronics