# K141529: Alviguide Blue+ Interventional Cardiology Guiding Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Alvimedica Tibbi Urunler Sanayi VE Dis Ticaret A.S
- Decided: Dec 3, 2014 after 177 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K981198 (1998). 11 ancestors in all.
No later device cites it as a predicate yet.
1 of 12 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062420: 5F Sherpa Active NX Guide Catheter, Medtronic Vascular (2006) Summary page 5.
- K021256: Z3 Guide Catheter, Medtronic Vascular (2002) Summary page 5.
- K022764: 7F Launcher Guide Catheter, Medtronic Vascular (2002) Summary page 5.
- K023402: 8F Launcher Guide Catheter, Medtronic Vascular (2002) Summary page 5.
- K043387: Vascon Polaris Guiding Catheter, Vascon, LLC (2005) Summary page 5.
- (no number) Medtronic 6F Launcher Guide Catheter: named in the summary without a submission number
- (no number) Merit Medical Systems Concierge Guiding Catheter: named in the summary without a submission number

## Indications for use
The Alviguide™ Blue+ Interventional Cardiology Guiding Catheter is intended for use in the intravascular introduction of interventional/diagnostic devices into the coronary vascular system. The Alguide™ Endovascular Guiding Catheter is intended for use in the intravascular introduction of interventional/diagnostic devices into the peripheral vascular system.

Source page: https://510kreport.com/device/K141529
Methodology: https://510kreport.com/methodology