# ClearStream Technologies, Ltd.

- Location (FDA's records): Wexford, IE
- FDA decisions: 7 (2008–2011): 7 510(k) clearances
- Product codes: LIT (5), DQY (2)
- Predicates its devices cite: 7 (6 its own); citations of its devices by later devices: 15 (6 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
- Invatec Innovative Technologies, S.R.L.: 1 (https://510kreport.com/company/invatec-innovative-technologies)

## Firms that cite its devices most
- Arravasc, Ltd.: 2 (https://510kreport.com/company/arravasc)
- Cordis US Corporation: 2 (https://510kreport.com/company/cordis-us)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Cordis Corp.: 1 (https://510kreport.com/company/cordis)
- Ev3, Inc.: 1 (https://510kreport.com/company/ev3)
- Invatec Innovative Technologies, S.R.L.: 1 (https://510kreport.com/company/invatec-innovative-technologies)
- Bard Peripheral Vascular, Inc.: 1 (https://510kreport.com/company/bard-peripheral-vascular)

## Its most-cited devices
- K072947: Savvy Long and Sleek Peripheral Transluminal Angioplasty (Pta) Catheters (2008), cited by 7
- K093139: Bantam,48XXXXXX, 50XXXXXX (2009), cited by 3
- K102035: Sleek Otw Pta Catheters (2010), cited by 2
- K083596: Reekross Family or Otw Pta Catheters (2009), cited by 1
- K112335: Bantam Catheter (280MM Balloon Lengths) (2011), cited by 1
- K100490: Litepac, Model 682 (2010), cited by 1

## Recent decisions
- K112335: Bantam Catheter (280MM Balloon Lengths) (Oct 12, 2011)
- K102035: Sleek Otw Pta Catheters (Dec 1, 2010)
- K101361: Reeflex Pta Catheter (Aug 4, 2010)
- K100490: Litepac, Model 682 (Mar 16, 2010)
- K093139: Bantam,48XXXXXX, 50XXXXXX (Dec 30, 2009)
- K083596: Reekross Family or Otw Pta Catheters (Mar 2, 2009)
- K072947: Savvy Long and Sleek Peripheral Transluminal Angioplasty (Pta) Catheters (Feb 8, 2008)

Source page: https://510kreport.com/company/clearstream-technologies