# Johnson & Johnson Interventional Systems

- Location (FDA's records): Warren, NJ
- FDA decisions: 2 (1991–1991): 2 510(k) clearances
- Product codes: FGE (1), DQY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 22 (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 that cite its devices most
- Cordis Corp.: 10 (https://510kreport.com/company/cordis)
- Intratherapeutics, Inc.: 8 (https://510kreport.com/company/intratherapeutics)
- Guidant Corp.: 3 (https://510kreport.com/company/guidant)
- Advanced Cardiovascular Systems, Inc.: 1 (https://510kreport.com/company/advanced-cardiovascular-systems)

## Its most-cited devices
- K911581: Palmaz (TM) Balloon-Expandable Stent, Modification (1991), cited by 12
- K905720: Palmaz Biliary Stent (1991), cited by 10

## Recent decisions
- K911581: Palmaz (TM) Balloon-Expandable Stent, Modification (Jun 4, 1991)
- K905720: Palmaz Biliary Stent (Feb 5, 1991)

Source page: https://510kreport.com/company/johnson-johnson-interventional-systems