# K001209: Insight Plus 9000 Phased Array Torso and Pelvis Coil

- Pathway: 510(k) (Traditional)
- Applicant: Usa Instruments, Inc.
- Decided: Jun 1, 2000 after 48 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.
18 later devices descend from it; 7 cite it directly.
0 of 19 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
- K033753: Pelvic Array Coil (2003), 4 descendants of its own
- K030495: 3.0T Torso Phased Array Coil (2003), 4 descendants of its own
- K031209: GE 1.5T 8 Channel Torso Coil (2003), 3 descendants of its own
- K061715: Mrgfus General Purpose and Breast Coil (2006), 2 descendants of its own

Source page: https://510kreport.com/device/K001209
Methodology: https://510kreport.com/methodology