# Intl. Diagnostic Technology

- Location (FDA's records): Mchenry, IL
- FDA decisions: 29 (1976–1985): 29 510(k) clearances
- Product codes: DHN (2), KTL (2), GLZ (2), GOL (2), DCK (1), DEI (1), JQW (1), DFT (1), DHR (1), DDI (1), GQH (1), KLS (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
- K850591: Fiax Toxo-M Antibodies Test Kit (Apr 30, 1985)
- K843570: Fiax Haptoglobin Test Kit (Oct 5, 1984)
- K843621: Fiax 420 Dilutor (Sep 28, 1984)
- K843356: Fiax 100 Fluorometer (Sep 17, 1984)
- K842749: Fiax Total Ige Test Kit (Aug 28, 1984)
- K842071: Fiax Transferrin Test Kit (Jul 11, 1984)
- K841174: Rubella Antibody Fluoroimmunoassay (Jun 7, 1984)
- K840867: Alpha-1-Antitrypsin, Fitc, Antigen (May 11, 1984)

Source page: https://510kreport.com/company/intl-diagnostic-technology