# K073236: Neocoil 3.0T 32-Channel Torso Array Coil for GE

- Pathway: 510(k) (Traditional)
- Applicant: Neocoil
- Decided: Nov 30, 2007 after 14 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 K971667 (1997). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030495: 3.0T Torso Phased Array Coil, Ge Medical Systems, Inc. (2003) Summary page 2.
- K031209: GE 1.5T 8 Channel Torso Coil, Ge Medical Systems, Inc. (2003) Summary page 1.

## Indications for use
The NeoCoil 3.OT 32-Channel Torso Array Coil is intended to be used in the abdomen, pelvis, and chest regions for 2D and 3D magnetic resonance imaging and parallel body imaging for use on 3.OT GE HD series Magnetic Resonance scanners.

Source page: https://510kreport.com/device/K073236
Methodology: https://510kreport.com/methodology