# K182590: 1.5T AIR MP M, 1.5T AIR MP L, 1.5T 16ch AIR AA, 1.5T 30ch AIR AA

- Pathway: 510(k) (Traditional)
- Applicant: GE Healthcare
- Decided: Oct 19, 2018 after 29 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 K172695 (2017). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K172695: AIR Anterior Array, AIR Posterior Array, Ge Healthcare Coils (Usa Instruments, Inc.) (2017) Summary page 5.

## Most influential descendants
- K223378: 3.0T 16ch AIR AA (2023), 0 descendants of its own

## Indications for use
The 1.5T AIR MP M, 1.5T AIR MP L, 1.5T 16ch AIR AA, and 1.5T 30ch AIR AA are receive only RF coils designed for use with GE 1.5T MRI systems to produce diagnostic images on general human anatomy including extremities. The nucleus detected is hydrogen.

Source page: https://510kreport.com/device/K182590
Methodology: https://510kreport.com/methodology