# Mediguide, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 3 (2009–2010): 3 510(k) clearances
- Product codes: DQK (2), DQO (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Biosense Webster, Inc.: 2 (https://510kreport.com/company/biosense-webster)
- Paieon, Inc.: 1 (https://510kreport.com/company/paieon)
- Stereotaxis, Inc.: 1 (https://510kreport.com/company/stereotaxis)
- Volcano Corporation: 1 (https://510kreport.com/company/volcano)
- Angiometrx, Inc.: 1 (https://510kreport.com/company/angiometrx)

## Firms that cite its devices most
- St. Jude Medical, Cardiac Rhythm Management Divisi: 2 (https://510kreport.com/company/st-jude-medical-cardiac-rhythm-management-divisi)
- St. Jude Medical, Mediguide Navigation Systems: 1 (https://510kreport.com/company/st-jude-medical-mediguide-navigation-systems)
- St Jude Medical: 1 (https://510kreport.com/company/st-jude-medical)

## Its most-cited devices
- K091781: Guided Medical Positioning System (GMPS) (2009), cited by 2
- K091780: Guided Measurement Catheter (GMC) (2009), cited by 1
- K102905: Guided Medical Positioning System II (GMPS II) (2010), cited by 1

## Recent decisions
- K102905: Guided Medical Positioning System II (GMPS II) (Oct 29, 2010)
- K091781: Guided Medical Positioning System (GMPS) (Oct 16, 2009)
- K091780: Guided Measurement Catheter (GMC) (Oct 16, 2009)

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