# K090613: CPS Aim SL Slittable Inner Catheters, Models DS2N021-59, DS2N022-59, DS2NO23-59, DS2N024-65, DS2N024-65, DS2N021-65, DS2

- Pathway: 510(k) (Special)
- Applicant: St. Jude Medical, Cardiac Rhythm Management Divisi
- Decided: Jul 1, 2009 after 117 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
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K130252: CPS Aim Universal Slittable Inner Catheter (2013), 1 descendant of its own
- K221750: CPS AIM Universal II Slittable Inner Catheter (2022), 0 descendants of its own
- K142235: CPS Aim MediGuide Enabled inner catheter, CPS Aim Mediguide Enabled inner Catheter (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K090613
Methodology: https://510kreport.com/methodology