# K073181: Neocoil 1.5T 16 Channel Cardiac-Abdominal-Pelvic Array Coil

- Pathway: 510(k) (Traditional)
- Applicant: Neocoil, LLC
- Decided: Nov 21, 2007 after 8 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 K041185 (2004). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041185: Torso Array Coil, Model 558GE-64, Igc-Medical Advances, Inc. (2004) Summary page 2.

## Indications for use
To be used inconjunction with 1.5T GE HD series Magnetic Resonance scanners to produce diagnostic images of the chest, abdominal, and pelvic regions that can be interpreted by a trained physician.

Source page: https://510kreport.com/device/K073181
Methodology: https://510kreport.com/methodology