# K103365: Discovery 3T 16 CH Body Array Coil (Anterior); Discovery 3T 16 CH Body Array Coil (Posterior); Discovery 3T 32 CH Body a

- Pathway: 510(k) (Traditional)
- Applicant: Ge Healthcare Coils (Usa Instruments, Inc.)
- Decided: Jan 12, 2011 after 56 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: 3 generations back to K001209 (2000). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030371: Prima Iii Totalsense Torso Coil, Usa Instruments, Inc. (2003) Summary page 1.

## Indications for use
The Discovery 3T 16 Ch Body Array Coil and Discovery 3T 32 Ch Body Array Coil are receive-only RIF Coils designed for use with 3.OT MRI systems manufactured by GE Healthcare. The indications for use include chgst, cardiac, abdomen, torso, pelvis, prostate, hips, and long bone imaging. The nucleus detected is hydrogen.

Source page: https://510kreport.com/device/K103365
Methodology: https://510kreport.com/methodology