# K193324: Motion Correction System

- Pathway: 510(k) (Traditional)
- Applicant: Kineticor, Inc.
- Decided: Feb 4, 2020 after 64 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- 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: 16 generations back to K971684 (1997). 38 ancestors in all.
2 later devices descend from it; 1 cites it directly.
6 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183254: Magnetom Vida, Siemens Medical Solutions USA, Inc. (2019) Summary page 5.

## Most influential descendants
- K203451: TCL3 Motion Tracking System (2021), 1 descendant of its own
- K221785: TCL3 Motion Tracking System (2022), 0 descendants of its own

## Indications for use
The Motion Correction System is an accessory to a Magnetic Resonance Imaging (MRI) scanner. The system is a sensor-based technology for tracking of patient movement during an MRI session. It provides the current position of the patient in real-time to the MRI scanner for further data processing. User: Professional Use Environment: Hospital, doctor’s office, or any facility that uses an MRI device KinetiCor defines the Motion Correction System as an accessory to a medical device. It is intended to support, supplement and/or augment the performance of the MAGNETOM Skyra 3T MRI scanner.

Source page: https://510kreport.com/device/K193324
Methodology: https://510kreport.com/methodology