# K022669: 8 Channel Cardiac Phased Array Coil

- Pathway: 510(k) (Special)
- Applicant: GE Medical Systems
- Decided: Sep 6, 2002 after 25 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: 1 generation back to K971667 (1997). 2 ancestors in all.
5 later devices descend from it; 2 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K971667: Cardiac Phased Array Coil, GE Medical Systems (1997) Summary page 1.
- K013159: HRH-63-8 Head Array Coil, Mri Devices Corp. (2001)

## Most influential descendants
- K031209: GE 1.5T 8 Channel Torso Coil (2003), 3 descendants of its own
- K052584: 1.5T 12 Channel Body Array (2005), 1 descendant of its own
- K032045: 8 Channel Cardiac Phased Array Coil (2003), 1 descendant of its own
- K101492: 8 Channel Cardiac Phased Array Coil (2010), 0 descendants of its own
- K073236: Neocoil 3.0T 32-Channel Torso Array Coil for GE (2007), 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/K022669
Methodology: https://510kreport.com/methodology