# Biodiagnostic Intl

- Location (FDA's records): Mchenry, IL
- FDA decisions: 11 (1983–2004): 11 510(k) clearances
- Product codes: JJY (3), DIF (2), LCP (1), KRZ (1), DKB (1), JIT (1), JJX (1), JJW (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
- K031296: Liqui-Heme Glyco A1C Assay (Oct 15, 2004)
- K881430: Liqui-Sera Serum Alcohol Controls (Jul 8, 1988)
- K874459: Liqui-Sera Spinal Fluid Control (Dec 29, 1987)
- K863849: Liqui-Sera Combo Ligand/TDM Controls (Nov 24, 1986)
- K853906: Liqui-Sera Chemistry Controls (Comprehensive) (Oct 4, 1985)
- K853887: Liqui-Sera Chem. Multiple Calibrators (Sep 30, 1985)
- K842668: Liqui-Heme Hemoglobin Calibrators (Mar 5, 1985)
- K840618: Liqui-Ura Chemistry Urine Controls (Apr 4, 1984)

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