# Boston Scientific/Medi-Tech

- Location (FDA's records): Natick,, MA
- FDA decisions: 5 (2001–2002): 5 510(k) clearances
- Product codes: DQO (2), MSD (1), DSY (1), FGE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 8 (0 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Boston Scientific Corp: 5 (https://510kreport.com/company/boston-scientific)
- Vascular Solutions, Inc.: 1 (https://510kreport.com/company/vascular-solutions)
- Angiotech: 1 (https://510kreport.com/company/angiotech)
- Navilyst Medical, Inc.: 1 (https://510kreport.com/company/navilyst-medical)

## Its most-cited devices
- K023870: Flexima Biliary Catheter (2002), cited by 4
- K011664: Imager II Angiographic Catheter (2001), cited by 3
- K020012: Modification to Renegade Fiber Braided Microcatheter (2002), cited by 1

## Recent decisions
- K023870: Flexima Biliary Catheter (Dec 20, 2002)
- K020012: Modification to Renegade Fiber Braided Microcatheter (Jan 29, 2002)
- K012948: Modification to Vaxcel Dialysis Catheter (Oct 3, 2001)
- K012952: Hemashield Gold Woven Double Velour Vascular Graft - Branch Graft (Oct 2, 2001)
- K011664: Imager II Angiographic Catheter (Sep 7, 2001)

Source page: https://510kreport.com/company/boston-scientific-medi-tech