# Qxmedical, LLC

- Location (FDA's records): Saint Paul, MN
- FDA decisions: 5 (2012–2020): 5 510(k) clearances
- Product codes: DQY (4), MJN (1)
- 510(k) review time since 2016: median 117 days, against 117 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 7 (2 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
- Spectranetics Corp.: 2 (https://510kreport.com/company/spectranetics)
- Vascular Solutions, Inc.: 1 (https://510kreport.com/company/vascular-solutions)
- Merit Medical Systems, Inc.: 1 (https://510kreport.com/company/merit-medical-systems)
- Via Biomedical, Inc.: 1 (https://510kreport.com/company/via-biomedical)

## Firms that cite its devices most
- Philips Image Guided Therapy Devices: 1 (https://510kreport.com/company/philips-image-guided-therapy-devices)
- Arch Catheter, LLC: 1 (https://510kreport.com/company/arch-catheter)
- W. L. Gore and Associates, Inc.: 1 (https://510kreport.com/company/w-l-gore-and-associates)
- Xablecath, Inc.: 1 (https://510kreport.com/company/xablecath)
- Renalpro Medical, Inc.: 1 (https://510kreport.com/company/renalpro-medical)

## Its most-cited devices
- K123311: Qxmedical Access & Support Catheter (2013), cited by 3
- K120381: Q50 Plus Stent Graft Balloon Catheter (2012), cited by 2
- K183679: Occlusion Balloon Catheter (2019), cited by 2

## Recent decisions
- K200317: Support Catheter (May 14, 2020)
- K183679: Occlusion Balloon Catheter (Apr 24, 2019)
- K160561: Boosting Catheter (Nov 2, 2016)
- K123311: Qxmedical Access & Support Catheter (Jan 14, 2013)
- K120381: Q50 Plus Stent Graft Balloon Catheter (Feb 24, 2012)

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