# K992892: Stepping Kinematic Imaging Platform (Skip)

- Pathway: 510(k) (Traditional)
- Applicant: Magnetic Moments, LLC
- Decided: Sep 16, 1999 after 20 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: 2 generations back to K945827 (1995). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K980645: Philips Gyroscan NT Release 6 Series, Philips Medical Systems North America, Inc. (1998) Summary page 1.
- K940541: Magnetic Resonance Diag Device Magnetom Vision (Modif), Siemens Medical Solutions USA, Inc. (1994) Summary page 1.
- K942604: Signa Advantage SP Magnetic Resonance System, GE Medical Systems (1995) Summary page 1.
- K931544: 1.5T Edge and 1.0T Vista Systems, Philips Medical Systems (Cleveland), Inc. (1993) Summary page 1.
- K960973: Movable Add-on Couch for Outlook, Philips Medical Systems (Cleveland), Inc. (1996) Summary page 2.

## Indications for use
The device is intended to translate (reposition) the patient manually within a magnetic resonance imaging machine, through the magnet bore, in order to center different regions-of-interest at the center of the magnetic field for either multistation MRA with single dose injection or multistation MRI, using existing system hardware, software and imaging coils.

Source page: https://510kreport.com/device/K992892
Methodology: https://510kreport.com/methodology