# Connecticut Diagnostics, Ltd.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1979–1991): 14 510(k) clearances
- Product codes: CIG (2), GGK (2), CED (1), CGA (1), JWX (1), KNK (1), CEK (1), CIC (1), GIF (1), CGX (1), JGZ (1), CIX (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
- K905617: Visi-Staph (Mar 29, 1991)
- K822504: CDL Auto-Lysing Reagent (Sep 17, 1982)
- K822500: CDL Lysing Reagent (Sep 17, 1982)
- K822501: CDL Isotonic Diluent (Sep 17, 1982)
- K811222: Inorganic Phosphorus Reagents (May 21, 1981)
- K801897: Glucose Diagnostic Reagent (Oct 10, 1980)
- K801898: Uric Acid Diagnostic Reagent (Oct 10, 1980)
- K792465: Connecticut Diagnostics, LTS. Direct (Dec 18, 1979)

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