# Bard Interventional Products Div.

- Location (FDA's records): Billerica, MA
- FDA decisions: 2 (1996–1998): 2 510(k) clearances
- Product codes: KNS (2)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (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
- Wiltek Medical, Inc.: 2 (https://510kreport.com/company/wiltek-medical)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)

## Firms that cite its devices most
- Conmed Endoscopic Technologies, Inc.: 1 (https://510kreport.com/company/conmed-endoscopic-technologies)

## Its most-cited devices
- K982557: Bard Proforma and Apollo Pre-Curved Papillotomes (1998), cited by 1

## Recent decisions
- K982557: Bard Proforma and Apollo Pre-Curved Papillotomes (Sep 10, 1998)
- K963484: Bard High Flow Papillotome (Nov 19, 1996)

Source page: https://510kreport.com/company/bard-interventional-products-div
