# K091703: HD Guide Catheter, Model 90019, 90022, 90023, 90120, 90121, 90130, 90131

- Pathway: 510(k) (Traditional)
- Applicant: Concentric Medical, Inc.
- Decided: Oct 14, 2009 after 126 days
- Product code: QEZ (Aspiration Thrombectomy Catheter)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K010579 (2001). 12 ancestors in all.
No later device cites it as a predicate yet.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073519: Quickcat Extraction Catheter, Model 60090-01, Kensey Nash Corp. (2008) Summary page 5.

## Indications for use
The HD Guide Catheter is indicated for the removal/aspiration of fresh, soft emboli and thrombi from vessels in the arterial system.

Source page: https://510kreport.com/device/K091703
Methodology: https://510kreport.com/methodology