# K032045: 8 Channel Cardiac Phased Array Coil

- Pathway: 510(k) (Special)
- Applicant: GE Medical Systems
- Decided: Jul 30, 2003 after 28 days
- Product code: MOS (Coil, Magnetic Resonance, Specialty)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K971667 (1997). 3 ancestors in all.
1 later device descends 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)
- K022669: 8 Channel Cardiac Phased Array Coil, GE Medical Systems (2002) Summary page 1.

## Most influential descendants
- K101492: 8 Channel Cardiac Phased Array Coil (2010), 0 descendants of its own

## Indications for use
It is intended to be used in the heart and mediastinum regions for 2D and 3D Magnetic Resonance imaging.

Source page: https://510kreport.com/device/K032045
Methodology: https://510kreport.com/methodology