# Intratherapeutics, Inc.

- Location (FDA's records): Saint Paul, MN
- FDA decisions: 15 (1998–2001): 15 510(k) clearances
- Product codes: FGE (11), JCT (2), DQY (2)
- Predicates its devices cite: 21 (5 its own); citations of its devices by later devices: 12 (5 its own)
- Recalls linked to its devices: 13 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Johnson & Johnson Interventional Systems: 8 (https://510kreport.com/company/johnson-johnson-interventional-systems)
- Cordis Corp.: 6 (https://510kreport.com/company/cordis)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Boston Scientific Scimed, Inc.: 1 (https://510kreport.com/company/boston-scientific-scimed)

## Firms that cite its devices most
- Sulzer Intratherapeutics, Inc.: 7 (https://510kreport.com/company/sulzer-intratherapeutics)

## Its most-cited devices
- K991929: Intrastent (1999), cited by 3
- K003040: Intrastent Protege Self-Expanding Nitinol Stent with Starport Delivery Technology (2000), cited by 3
- K980290: Iti Stent (1998), cited by 2
- K990221: Intracoil Peripheral Stent (1999), cited by 1
- K993904: Intrastent Doublestrut LD (2000), cited by 1
- K001257: Intracoil Stent (2000), cited by 1

## Recent decisions
- K011184: Intrastent Doublestrut Paramount XS Biliary Endoprosthesis (Aug 13, 2001)
- K003997: Intrastent Doublestrut Paramount XS Biliary Endoprosthesis (Jan 24, 2001)
- K003040: Intrastent Protege Self-Expanding Nitinol Stent with Starport Delivery Technology (Dec 28, 2000)
- K003450: Intrastent Doublestrut Paramount Biliary Endoprosthesis (Dec 7, 2000)
- K001648: Intrastent Doublestrut Paramount (Aug 28, 2000)
- K001257: Intracoil Stent (May 18, 2000)
- K000864: Intrastent Doublestrut XS Stent (Apr 14, 2000)
- K993904: Intrastent Doublestrut LD (Feb 1, 2000)

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