# Xtrak Medical, Inc.

- Location (FDA's records): Hopkonton, MA
- FDA decisions: 3 (2002–2003): 3 510(k) clearances
- Product codes: DQY (1), MCW (1), QEW (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (1 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
- Intra Luminal Therapeutics, Inc.: 1 (https://510kreport.com/company/intra-luminal-therapeutics)
- Possis Medical, Inc.: 1 (https://510kreport.com/company/possis-medical)
- Arrow Intl., Inc.: 1 (https://510kreport.com/company/arrow-intl)

## Firms that cite its devices most
- Asahi Intecc Co., Ltd.: 1 (https://510kreport.com/company/asahi-intecc)

## Its most-cited devices
- K032660: Xtrak Support Catheter (2003), cited by 1
- K013473: XTD Thrombectomy Catheter, XX CM, Model# CT000500X; XTD Control Console, Model # CT0006001; XTD Collection Bottle, Model (2002), cited by 1

## Recent decisions
- K032660: Xtrak Support Catheter (Oct 29, 2003)
- K021641: XTD Thrombectomy Catheter, XX CM (Jul 26, 2002)
- K013473: XTD Thrombectomy Catheter, XX CM, Model# CT000500X; XTD Control Console, Model # CT0006001; XTD Collection Bottle, Model (Mar 6, 2002)

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