# Anco Medical Reagents & Assoc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 26 (1981–1984): 26 510(k) clearances
- Product codes: GHM (2), JIS (2), CGE (1), CDT (1), CIG (1), LFQ (1), KHG (1), CEK (1), CIQ (1), CFD (1), CDW (1), JPK (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
- K842440: Sickle Cell Stat a/S Heterozygous-Eryth (Jul 27, 1984)
- K831871: Sickle-Heme a/S Controls & a/a Control (Jul 28, 1983)
- K821658: Hemoglobin Reagent (Jun 25, 1982)
- K821526: Acid Phosphatase Reagent Set (Jun 10, 1982)
- K821102: Megnesium Reagent Kit (May 5, 1982)
- K820951: Enzymatic Cholesterol Kit (Apr 26, 1982)
- K820466: Sgot Reagent Set (Mar 11, 1982)
- K820500: Total Lipid Reagent Set (Mar 11, 1982)

Source page: https://510kreport.com/company/anco-medical-reagents-assoc