# K062531: Angioguard XP Emboli Capture Guidewire and Angioguard RX Emboli Capture Guidewire

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp., A Johnson & Johnson Co.
- Decided: Sep 22, 2006 after 24 days
- Product code: NTE (Temporary Carotid Catheter For Embolic Capture)
- 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
No predicates in its family tree.
6 later devices descend from it; 2 cite it directly.
2 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) FilterWire EX Embolic Protection System: named in the summary without a submission number
- (no number) PercuSurge GuardWire Temporary Occlusion and Aspiration System: named in the summary without a submission number

## Most influential descendants
- K101651: Angioguard XP Emboli Capture Guidewire, Angioguard RX Emboli Capture Guidewire (2010), 5 descendants of its own
- K143570: Wirion (2015), 3 descendants of its own
- K180023: Wirion (2018), 2 descendants of its own
- K200198: Wirion (2020), 1 descendant of its own
- K220654: ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire (2022), 0 descendants of its own

## Indications for use
The ANGIOGUARD XP Emboli Capture Guidewire is indicated for use as a guidewire and embolic protection system to contain and remove embolic material (thrombus/debris) while performing carotid artery angioplasty and stenting procedures in carotid arteries. The diameter of the artery at the site of filter basket placement should be from 3mm to 7.5 mm.

Source page: https://510kreport.com/device/K062531
Methodology: https://510kreport.com/methodology