# K172394: Steerable Guide Catheter

- Pathway: 510(k) (Special)
- Applicant: Abbott Vascular
- Decided: Sep 6, 2017 after 29 days
- Product code: DRA (Catheter, Steerable)
- Device class: 2
- Regulation: 21 CFR 870.1280
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 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 no predicate by number.

## Most influential descendants
- K190167: MitraClip G4 Steerable Guide Catheter (2019), 3 descendants of its own
- K221397: MitraClip G4 Steerable Guide Catheter (2022), 2 descendants of its own
- K241538: TriClip Steerable Guide Catheter (2024), 1 descendant of its own
- K243224: MitraClip™ G5 Steerable Guide Catheter (SGC0801); TriClip™ G5 Steerable Guide Catheter (TSGC0801) (2024), 0 descendants of its own

Source page: https://510kreport.com/device/K172394
Methodology: https://510kreport.com/methodology