# K002482: Vision 9000 Phased Array Torso Coil

- Pathway: 510(k) (Traditional)
- Applicant: Usa Instruments, Inc.
- Decided: Oct 17, 2000 after 64 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
No predicates in its family tree.
7 later devices descend from it; 1 cites 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K013594: Body Array Coil (2002), 6 descendants of its own
- K024187: Spirit Iii Totalsense Cardiac Coil (2003), 2 descendants of its own
- K031172: Spirit Iii Totalsense Cardiac Coil (2003), 1 descendant of its own
- K030371: Prima Iii Totalsense Torso Coil (2003), 1 descendant of its own
- K103365: Discovery 3T 16 CH Body Array Coil (Anterior); Discovery 3T 16 CH Body Array Coil (Posterior); Discovery 3T 32 CH Body a (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K002482
Methodology: https://510kreport.com/methodology