# K162946: 8ch Knee-Foot SPEEDER

- Pathway: 510(k) (Traditional)
- Applicant: Quality Electrodynamics, LLC
- Decided: Jan 6, 2017 after 77 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 K152695 (2015). 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)
- K152695: 8 CH Knee SPEEDER, Quality Electrodynamics, LLC (2015) Summary page 4.

## Indications for use
The 8ch Knee-Foot SPEEDER Coil is intended for use with Toshiba 1.5T MR systems to produce diagnostic images of the knee, wrist, hand, foot and ankle that can be interpreted by a trained physician.

Source page: https://510kreport.com/device/K162946
Methodology: https://510kreport.com/methodology