# Biocheck, Inc.

- Location (FDA's records): Northridge, CA
- FDA decisions: 14 (1999–2004): 14 510(k) clearances
- Product codes: MMI (2), JLW (2), DCN (1), KLI (1), JZG (1), DGC (1), CDP (1), DCK (1), JHI (1), CDZ (1), DBF (1), DRR (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Vancouver Biotech, Ltd.: 1 (https://510kreport.com/company/vancouver-biotech)

## Recent decisions
- K041619: Bio Check Whole Blood/Plasma/Sermon Model #801116 (Dec 17, 2004)
- K040030: Biocheck Cardiac-1 CRP Rapid Test, Model BC-804114 (Jun 16, 2004)
- K022660: Biocheck Myoglobin Elisa, Model BC-1117 (Dec 19, 2002)
- K013062: Biocheck Human Cardiac Troponin-I Immunoassay Test Kit (Jan 8, 2002)
- K003851: Biocheck High Sensitivity C-Reactive Protein Enzyme Immunoassay Test Kit, Model BC-1119 (Jul 20, 2001)
- K002294: Biocheck Testosterone Eia, Model BC-1115 (Oct 2, 2000)
- K001022: Biocheck, Inc. B-2 Microglobin Enzyme Immunoasay Test Kit, Model BC-1061 (Sep 26, 2000)
- K992517: Biocheck Ferritin Elisa Model BC-1025 (Sep 24, 1999)

Source page: https://510kreport.com/company/biocheck