# Centurion Medical Products Corporation

- Location (FDA's records): Williamston, MI
- FDA decisions: 3 (2011–2022): 3 510(k) clearances
- Names in FDA's records: Centurion Medical Products Corporation (2); Centurion Medical Products (1)
- Product codes: DRS (1), DQX (1), FPA (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mirador Biomedical, Inc.: 1 (https://510kreport.com/company/mirador-biomedical)
- Health Line International Corporation: 1 (https://510kreport.com/company/health-line-international)
- Arrow Intl., Inc.: 1 (https://510kreport.com/company/arrow-intl)
- Cardinal Health, Alaris Products: 1 (https://510kreport.com/company/cardinal-health-alaris-products)

## Firms that cite its devices most
- Busse Hospital Disposables, Inc.: 1 (https://510kreport.com/company/busse-hospital-disposables)

## Its most-cited devices
- K103562: Centurion Pressure Injectable Extension Set (2011), cited by 1

## Recent decisions
- K210548: Medline Integrated Arterial Catheter (May 17, 2022)
- K161408: Compass Cast and MAP (Nov 22, 2016)
- K103562: Centurion Pressure Injectable Extension Set (Jun 23, 2011)

Source page: https://510kreport.com/company/centurion-medical-products