# R4 Vascular, Inc.

- Location (FDA's records): Maple Grove, MN
- FDA decisions: 7 (2007–2013): 7 510(k) clearances
- Product codes: LJS (3), MSD (2), LIT (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 6 (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
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Medcomp: 1 (https://510kreport.com/company/medcomp)

## Firms that cite its devices most
- Semprus Biosciences: 2 (https://510kreport.com/company/semprus-biosciences)
- Arrow International, Inc. (Subsidiary of Teleflex, Inc.): 1 (https://510kreport.com/company/arrow-international-subsidiary-of-teleflex)
- Vector Corporation, LLC: 1 (https://510kreport.com/company/vector)
- Navilyst Medical, Inc.: 1 (https://510kreport.com/company/navilyst-medical)

## Its most-cited devices
- K083763: Zeus CT Picc 4 FR and 5 FR Single and Dual Lumen (2009), cited by 3
- K091506: Duraspan Hemodialysis Long-Term Catheter, Models 62152420, 621512820, 62153220, 62153620, 62154020, 62155520 (2010), cited by 1
- K121385: Vector (2012), cited by 1
- K131329: Vector Pta Balloon Dilatation Catheter (2013), cited by 1

## Recent decisions
- K131329: Vector Pta Balloon Dilatation Catheter (Jun 6, 2013)
- K121385: Vector (Jun 14, 2012)
- K100169: Duraspan Hemodialysis Long-Term Catheter (Feb 18, 2010)
- K091506: Duraspan Hemodialysis Long-Term Catheter, Models 62152420, 621512820, 62153220, 62153620, 62154020, 62155520 (Jan 8, 2010)
- K092040: Pherocious 10.5 FR (24 CM, 28 CM and 32 CM), Models 430102440, 430102840, 430103240 (Nov 18, 2009)
- K083763: Zeus CT Picc 4 FR and 5 FR Single and Dual Lumen (Mar 16, 2009)
- K071361: R4 Vascular Inc. Pegasus CT Picc, Model 500005-001,002, 004, 005, 500004-001, 002,004,005 (Aug 20, 2007)

Source page: https://510kreport.com/company/r4-vascular