# Princeton Biomedix

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1976–1995): 14 510(k) clearances
- Product codes: JHI (3), CGA (1), DDR (1), DHA (1), CFJ (1), KTN (1), CJE (1), CJR (1), LFX (1), CEP (1), LCX (1), JPZ (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
- K942052: Lifesign MI Myoglobin (Feb 7, 1995)
- K925355: Biosign (TM_ Rubella - Rubella Antibody Test (Jul 12, 1994)
- K930185: Ovusign LH/Conception Plus/Ovudate LH One-Step (Mar 4, 1993)
- K925183: Biosign (TM) Mono-Infect Mono Hetero Antibody Test (Feb 23, 1993)
- K926308: Lifesign HCG - One Step Home Pregnancy Test (Jan 26, 1993)
- K901011: Biosign HCG-One Step Pregnancy Test (May 4, 1990)
- K894705: Biospot HCG-Rapid Pregnancy Test (Oct 18, 1989)
- K894750: Biostix I. HCG - One Step Pregnancy Test (Oct 18, 1989)

Source page: https://510kreport.com/company/princeton-biomedix