# K123272: 1.5T 16CH Flex Speeder Large, 1.5T 16CH Flex Speeder Medium

- Pathway: 510(k) (Abbreviated)
- Applicant: Neocoil, LLC
- Decided: Mar 28, 2013 after 160 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: 3 generations back to K101632 (2010). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121362: 1.5T 16CH Flex Speeder Large, Neocoil, LLC (2012) Summary page 1.

## Indications for use
To be used in conjunction with Toshiba 1.5T Magnetic Resonance Scanners with DL96 connectors to produce diagnostic images of the upper and lower extremities, chest, abdomen, pelvis, head, neck and spine in pediatric and adult populations that can be interpreted by a trained physician.

Source page: https://510kreport.com/device/K123272
Methodology: https://510kreport.com/methodology