# K023110: Cedars-Sinai Motion Correction (Moco) Software, Model 111005

- Pathway: 510(k) (Traditional)
- Applicant: Digirad Corp.
- Decided: Nov 22, 2002 after 64 days
- Product code: KPS (System, Tomography, Computed, Emission)
- Device class: 2
- Regulation: 21 CFR 892.1200
- 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 K003264 (2000). 2 ancestors in all.
9 later devices descend from it; 2 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010509: Cedars-Sinai BPGS and Moco, Smv America (2001)
- K003264: QPS/BPGS/Moco Processing Applications for Entegra Workstation, Ge Medical Systems F.I. Haifa (2000)

## Most influential descendants
- K052430: Cardius-1, Cardius-2, Cardius-3, 2020TC Spect Imaging System (2005), 7 descendants of its own
- K070542: Cardius 1, 2 and 3 Xpo and 2020TC Spect Imaging Systems (2007), 6 descendants of its own
- K100838: Ergo Imaging System (2010), 2 descendants of its own
- K082368: Cardius-1, -2, -3, and Cardius 1,2,3 Xpo Spect Imaging Systems, 2020TC Spect Imaging System (2008), 1 descendant of its own
- K123408: Ergo Imaging System (2013), 0 descendants of its own

## Indications for use
The Cedars-Sinai Motion Correction (MoCo) software program is intended for use in correcting patient motion artifacts in SPECT data acquired on a nuclear medicine gamma camera system.

Source page: https://510kreport.com/device/K023110
Methodology: https://510kreport.com/methodology