# Intracel Corp.

- Location (FDA's records): Rockville, MD
- FDA decisions: 5 (1995–2000): 5 510(k) clearances
- Product codes: LLH (1), GNW (1), GQH (1), MJH (1), GKZ (1)
- Predicates its devices cite: 2 (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
- Baxter Diagnostics, Inc.: 1 (https://510kreport.com/company/baxter-diagnostics)
- Biotest Diagnostics Corp.: 1 (https://510kreport.com/company/biotest-diagnostics)

## Recent decisions
- K003204: Bartels Viral Respiratory Screening and Identification Kit (Nov 7, 2000)
- K991074: Bartels Legionella Urinary Antigen Elisa Test (Dec 21, 1999)
- K990664: Prima System - Old, Bartels Elisa - New (Mar 31, 1999)
- K982311: Bartels Cinakit CMV Antigenemia (Dec 14, 1998)
- K933878: Zymmune (TM) CD4/CD8 Cell Monitoring Kit (Nov 14, 1995)

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