# K070238: Amplatzer Reliant Catheter Delivery System

- Pathway: 510(k) (Traditional)
- Applicant: Aga Medical Corp.
- Decided: Feb 28, 2007 after 34 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 K893658 (1989). 38 ancestors in all.
No later device cites it as a predicate yet.
0 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033989: Medtronic Selectsite Deflectable Catheter System, Models C304-S59 and C304-L69, Medtronic Inc. Cardiac Rhythm Management (2004) Summary page 2.

## Indications for use
The AMPLATZER® Reliant® Catheter Delivery System is intended to provide a pathway through which diagnostic and therapeutic transvenous devices are introduced within the chambers and coronary vasculature of the heart.

Source page: https://510kreport.com/device/K070238
Methodology: https://510kreport.com/methodology