# K183161: SnapShot Freeze 2

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems, LLC
- Decided: Feb 13, 2019 after 90 days
- Product code: JAK (System, X-Ray, Tomography, Computed)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K000315 (2000). 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)
- K120910: Cardiq Xpress 2.0 with Snapshot Freeze Option Cardiq Xpress 2.0 Reveal, GE Medical Systems SCS (2012) Summary page 6.

## Indications for use
SnapShot Freeze 2 is designed for use with gated cardiac acquisitions to reduce cardiac induced motion artifacts.

Source page: https://510kreport.com/device/K183161
Methodology: https://510kreport.com/methodology