# Angioslide, Ltd.

- Location (FDA's records): Wheat Ridge, CO
- FDA decisions: 6 (2010–2017): 6 510(k) clearances
- Product codes: LIT (5), DQY (1)
- Predicates its devices cite: 9 (5 its own); citations of its devices by later devices: 7 (5 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
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)
- Ev3, Inc.: 1 (https://510kreport.com/company/ev3)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)

## Firms that cite its devices most
- Contego Medical, Inc.: 1 (https://510kreport.com/company/contego-medical)
- Ev3, Inc.: 1 (https://510kreport.com/company/ev3)

## Its most-cited devices
- K090364: Extra Pta Balloon Catheter with Embolic Protection Feature (2010), cited by 2
- K111750: Extra Pta Balloon Catheter with Embolic Capture Feature; Proteus Pta Balloon Catheter with Embolic Capture Feature (2011), cited by 2
- K133043: Proteus Pta Balloon Catheter with Embolic Capture Feature (2013), cited by 1
- K120805: Proteus Pta Balloon Catheter with Embolic Capture Feature (2012), cited by 1
- K172494: PROTEUS PTA Balloon Catheter with Embolic Capture Feature (2017), cited by 1

## Recent decisions
- K172494: PROTEUS PTA Balloon Catheter with Embolic Capture Feature (Dec 15, 2017)
- K133043: Proteus Pta Balloon Catheter with Embolic Capture Feature (Dec 6, 2013)
- K120164: Proteus Pta Balloon Catheter with Embolic Capture Feature (Jun 8, 2012)
- K120805: Proteus Pta Balloon Catheter with Embolic Capture Feature (Apr 13, 2012)
- K111750: Extra Pta Balloon Catheter with Embolic Capture Feature; Proteus Pta Balloon Catheter with Embolic Capture Feature (Jul 21, 2011)
- K090364: Extra Pta Balloon Catheter with Embolic Protection Feature (Mar 23, 2010)

Source page: https://510kreport.com/company/angioslide